Class: GeneAsAModelOfDiseaseAssociation
classDiagram
class GeneAsAModelOfDiseaseAssociation
ModelToDiseaseAssociationMixin <|-- GeneAsAModelOfDiseaseAssociation
EntityToDiseaseAssociationMixin <|-- GeneAsAModelOfDiseaseAssociation
GeneToDiseaseAssociation <|-- GeneAsAModelOfDiseaseAssociation
GeneAsAModelOfDiseaseAssociation : adjusted_p_value
GeneAsAModelOfDiseaseAssociation : agent_type
GeneAsAModelOfDiseaseAssociation --|> AgentTypeEnum : agent_type
GeneAsAModelOfDiseaseAssociation : aggregator_knowledge_source
GeneAsAModelOfDiseaseAssociation : anatomical_context_qualifier
GeneAsAModelOfDiseaseAssociation : category
GeneAsAModelOfDiseaseAssociation : deprecated
GeneAsAModelOfDiseaseAssociation : description
GeneAsAModelOfDiseaseAssociation : disease_context_qualifier
GeneAsAModelOfDiseaseAssociation --|> Disease : disease_context_qualifier
GeneAsAModelOfDiseaseAssociation : frequency_qualifier
GeneAsAModelOfDiseaseAssociation : has_attribute
GeneAsAModelOfDiseaseAssociation --|> Attribute : has_attribute
GeneAsAModelOfDiseaseAssociation : has_count
GeneAsAModelOfDiseaseAssociation : has_evidence
GeneAsAModelOfDiseaseAssociation --|> EvidenceType : has_evidence
GeneAsAModelOfDiseaseAssociation : has_percentage
GeneAsAModelOfDiseaseAssociation : has_quotient
GeneAsAModelOfDiseaseAssociation : has_supporting_studies
GeneAsAModelOfDiseaseAssociation --|> Study : has_supporting_studies
GeneAsAModelOfDiseaseAssociation : has_total
GeneAsAModelOfDiseaseAssociation : id
GeneAsAModelOfDiseaseAssociation : iri
GeneAsAModelOfDiseaseAssociation : knowledge_level
GeneAsAModelOfDiseaseAssociation --|> KnowledgeLevelEnum : knowledge_level
GeneAsAModelOfDiseaseAssociation : knowledge_source
GeneAsAModelOfDiseaseAssociation : name
GeneAsAModelOfDiseaseAssociation : negated
GeneAsAModelOfDiseaseAssociation : object
GeneAsAModelOfDiseaseAssociation --|> Disease : object
GeneAsAModelOfDiseaseAssociation : object_aspect_qualifier
GeneAsAModelOfDiseaseAssociation : object_category
GeneAsAModelOfDiseaseAssociation --|> OntologyClass : object_category
GeneAsAModelOfDiseaseAssociation : object_category_closure
GeneAsAModelOfDiseaseAssociation --|> OntologyClass : object_category_closure
GeneAsAModelOfDiseaseAssociation : object_closure
GeneAsAModelOfDiseaseAssociation : object_direction_qualifier
GeneAsAModelOfDiseaseAssociation --|> DirectionQualifierEnum : object_direction_qualifier
GeneAsAModelOfDiseaseAssociation : object_label_closure
GeneAsAModelOfDiseaseAssociation : object_namespace
GeneAsAModelOfDiseaseAssociation : object_specialization_qualifier
GeneAsAModelOfDiseaseAssociation : original_object
GeneAsAModelOfDiseaseAssociation : original_predicate
GeneAsAModelOfDiseaseAssociation : original_subject
GeneAsAModelOfDiseaseAssociation : p_value
GeneAsAModelOfDiseaseAssociation : predicate
GeneAsAModelOfDiseaseAssociation : primary_knowledge_source
GeneAsAModelOfDiseaseAssociation : publications
GeneAsAModelOfDiseaseAssociation --|> Publication : publications
GeneAsAModelOfDiseaseAssociation : qualified_predicate
GeneAsAModelOfDiseaseAssociation : qualifier
GeneAsAModelOfDiseaseAssociation : qualifiers
GeneAsAModelOfDiseaseAssociation --|> OntologyClass : qualifiers
GeneAsAModelOfDiseaseAssociation : retrieval_source_ids
GeneAsAModelOfDiseaseAssociation --|> RetrievalSource : retrieval_source_ids
GeneAsAModelOfDiseaseAssociation : sex_qualifier
GeneAsAModelOfDiseaseAssociation --|> BiologicalSex : sex_qualifier
GeneAsAModelOfDiseaseAssociation : subject
GeneAsAModelOfDiseaseAssociation --|> GeneOrGeneProduct : subject
GeneAsAModelOfDiseaseAssociation : subject_aspect_qualifier
GeneAsAModelOfDiseaseAssociation --|> GeneOrGeneProductOrChemicalEntityAspectEnum : subject_aspect_qualifier
GeneAsAModelOfDiseaseAssociation : subject_category
GeneAsAModelOfDiseaseAssociation --|> OntologyClass : subject_category
GeneAsAModelOfDiseaseAssociation : subject_category_closure
GeneAsAModelOfDiseaseAssociation --|> OntologyClass : subject_category_closure
GeneAsAModelOfDiseaseAssociation : subject_closure
GeneAsAModelOfDiseaseAssociation : subject_direction_qualifier
GeneAsAModelOfDiseaseAssociation --|> DirectionQualifierEnum : subject_direction_qualifier
GeneAsAModelOfDiseaseAssociation : subject_label_closure
GeneAsAModelOfDiseaseAssociation : subject_namespace
GeneAsAModelOfDiseaseAssociation : subject_specialization_qualifier
GeneAsAModelOfDiseaseAssociation : timepoint
GeneAsAModelOfDiseaseAssociation : type
Inheritance
- Entity
- Association
- GeneToDiseaseOrPhenotypicFeatureAssociation [ EntityToPhenotypicFeatureAssociationMixin GeneToEntityAssociationMixin]
- GeneToDiseaseAssociation [ EntityToDiseaseAssociationMixin GeneToEntityAssociationMixin]
- GeneAsAModelOfDiseaseAssociation [ ModelToDiseaseAssociationMixin EntityToDiseaseAssociationMixin]
- GeneToDiseaseAssociation [ EntityToDiseaseAssociationMixin GeneToEntityAssociationMixin]
- GeneToDiseaseOrPhenotypicFeatureAssociation [ EntityToPhenotypicFeatureAssociationMixin GeneToEntityAssociationMixin]
- Association
Slots
Name | Cardinality and Range | Inheritance | Examples |
---|---|---|---|
subject: A gene that has a role in modeling the disease. This may be a model organism ortholog of a known disease gene, or it may be a gene whose mutants recapitulate core features of the disease. |
1 GeneOrGeneProduct |
GeneToEntityAssociationMixin, FrequencyQualifierMixin, EntityToPhenotypicFeatureAssociationMixin, ModelToDiseaseAssociationMixin, Association | HGNC:2197 |
predicate: The relationship to the disease |
1 PredicateType |
GeneToEntityAssociationMixin, FrequencyQualifierMixin, EntityToPhenotypicFeatureAssociationMixin, ModelToDiseaseAssociationMixin, Association | |
object: disease |
1 Disease |
GeneToEntityAssociationMixin, FrequencyQualifierMixin, EntityToPhenotypicFeatureAssociationMixin, ModelToDiseaseAssociationMixin, Association | MONDO:0020066 |
subject_aspect_qualifier: Composes with the core concept to describe new concepts of a different ontological type. e.g. a process in which the core concept participates, a function/activity/role held by the core concept, or a characteristic/quality that inheres in the core concept. The purpose of the aspect slot is to indicate what aspect is being affected in an 'affects' association. This qualifier specifies a change in the subject of an association (aka: statement). |
0..1 GeneOrGeneProductOrChemicalEntityAspectEnum |
GeneToDiseaseOrPhenotypicFeatureAssociation, EntityToFeatureOrDiseaseQualifiersMixin | stability, abundance, expression, exposure |
object_direction_qualifier: Composes with the core concept (+ aspect if provided) to describe a change in its direction or degree. This qualifier qualifies the object of an association (aka: statement). |
0..1 DirectionQualifierEnum |
GeneToDiseaseOrPhenotypicFeatureAssociation, EntityToFeatureOrDiseaseQualifiersMixin | |
sex_qualifier: a qualifier used in a phenotypic association to state whether the association is specific to a particular sex. |
0..1 BiologicalSex |
EntityToPhenotypicFeatureAssociationMixin | |
disease_context_qualifier: A context qualifier representing a disease or condition in which a relationship expressed in an association took place. |
0..1 Disease |
EntityToPhenotypicFeatureAssociationMixin, EntityToFeatureOrDiseaseQualifiersMixin | MONDO:0004979, MONDO:0005148 |
subject_specialization_qualifier: A qualifier that composes with a core subject/object concept to define a more specific version of the subject concept, specifically using an ontology term that is not a subclass or descendant of the core concept and in the vast majority of cases, is of a different ontological namespace than the category or namespace of the subject identifier. |
0..1 Uriorcurie |
EntityToPhenotypicFeatureAssociationMixin | |
object_specialization_qualifier: A qualifier that composes with a core subject/object concept to define a more specific version of the subject concept, specifically using an ontology term that is not a subclass or descendant of the core concept and in the vast majority of cases, is of a different ontological namespace than the category or namespace of the subject identifier. |
0..1 Uriorcurie |
EntityToPhenotypicFeatureAssociationMixin | |
anatomical_context_qualifier: A statement qualifier representing an anatomical location where an relationship expressed in an association took place (can be a tissue, cell type, or sub-cellular location). |
0..1 String |
EntityToPhenotypicFeatureAssociationMixin | blood, cerebral cortext |
negated: if set to true, then the association is negated i.e. is not true |
0..1 Boolean |
Association | |
qualifier: grouping slot for all qualifiers on an edge. useful for testing compliance with association classes |
0..1 String |
Association | |
qualifiers: connects an association to qualifiers that modify or qualify the meaning of that association |
* OntologyClass |
Association | |
publications: One or more publications that report the statement expressed in an Association, or provide information used as evidence supporting this statement. |
* Publication |
Association | |
has_evidence: connects an association to an instance of supporting evidence |
* EvidenceType |
Association | |
knowledge_source: An Information Resource from which the knowledge expressed in an Association was retrieved, directly or indirectly. This can be any resource through which the knowledge passed on its way to its currently serialized form. In practice, implementers should use one of the more specific subtypes of this generic property. |
0..1 String |
Association | |
primary_knowledge_source: The most upstream source of the knowledge expressed in an Association that an implementer can identify. Performing a rigorous analysis of upstream data providers is expected; every effort is made to catalog the most upstream source of data in this property. Only one data source should be declared primary in any association. "aggregator knowledge source" can be used to capture non-primary sources. |
0..1 String |
Association | |
aggregator_knowledge_source: An intermediate aggregator resource from which knowledge expressed in an Association was retrieved downstream of the original source, on its path to its current serialized form. |
* String |
Association | |
knowledge_level: Describes the level of knowledge expressed in a statement, based on the reasoning or analysis methods used to generate the statement, or the scope or specificity of what the statement expresses to be true. |
1 KnowledgeLevelEnum |
Association | knowledge_assertion, prediction, statistical_association |
agent_type: Describes the high-level category of agent who originally generated a statement of knowledge or other type of information. |
1 AgentTypeEnum |
Association | manual_agent, automated_agent, computational_model, text_mining_agent |
timepoint: a point in time |
0..1 TimeType |
Association | |
original_subject: used to hold the original subject of a relation (or predicate) that an external knowledge source uses before transformation to match the biolink-model specification. |
0..1 String |
Association | |
original_predicate: used to hold the original relation/predicate that an external knowledge source uses before transformation to match the biolink-model specification. |
0..1 Uriorcurie |
Association | |
original_object: used to hold the original object of a relation (or predicate) that an external knowledge source uses before transformation to match the biolink-model specification. |
0..1 String |
Association | |
subject_category: Used to hold the biolink class/category of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
0..1 OntologyClass |
Association | biolink:Gene |
object_category: Used to hold the biolink class/category of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
0..1 OntologyClass |
Association | biolink:Disease |
subject_closure: Used to hold the subject closure of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
* String |
Association | |
object_closure: Used to hold the object closure of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
* String |
Association | ['MONDO:0000167', 'MONDO:0005395'] |
subject_category_closure: Used to hold the subject category closure of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
* OntologyClass |
Association | ['biolink:Gene", "biolink:NamedThing'] |
object_category_closure: Used to hold the object category closure of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
* OntologyClass |
Association | ['biolink:Disease", "biolink:NamedThing'] |
subject_namespace: Used to hold the subject namespace of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
0..1 String |
Association | NCBIGene |
object_namespace: Used to hold the object namespace of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
0..1 String |
Association | MONDO |
subject_label_closure: Used to hold the subject label closure of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
* String |
Association | ['BRACA1'] |
object_label_closure: Used to hold the object label closure of an association. This is a denormalized field used primarily in the SQL serialization of a knowledge graph via KGX. |
* String |
Association | breast cancer, cancer |
retrieval_source_ids: A list of retrieval sources that served as a source of knowledge expressed in an Edge, or a source of data used to generate this knowledge. |
* RetrievalSource |
Association | |
p_value: A quantitative confidence value that represents the probability of obtaining a result at least as extreme as that actually obtained, assuming that the actual value was the result of chance alone. |
0..1 Float |
Association | |
adjusted_p_value: The adjusted p-value is the probability of obtaining test results at least as extreme as the results actually observed, under the assumption that the null hypothesis is correct, adjusted for multiple comparisons. P is always italicized and capitalized. The actual P value* should be expressed (P=. 04) rather than expressing a statement of inequality (P<. 05), unless P<. |
0..1 Float |
Association | |
has_supporting_studies: A study that produced information used as evidence to generate the knowledge expressed in an Association. |
* Study |
Association | |
id: A unique identifier for an entity. Must be either a CURIE shorthand for a URI or a complete URI |
1 String |
Entity | |
iri: An IRI for an entity. This is determined by the id using expansion rules. |
0..1 IriType |
Entity | |
category: Name of the high level ontology class in which this entity is categorized. Corresponds to the label for the biolink entity type class. In a neo4j database this MAY correspond to the neo4j label tag. In an RDF database it should be a biolink model class URI. This field is multi-valued. It should include values for ancestors of the biolink class; for example, a protein such as Shh would have category values biolink:Protein , biolink:GeneProduct , biolink:MolecularEntity . In an RDF database, nodes will typically have an rdf:type triples. This can be to the most specific biolink class, or potentially to a class more specific than something in biolink. For example, a sequence feature f may have a rdf:type assertion to a SO class such as TF_binding_site, which is more specific than anything in biolink. Here we would have categories {biolink:GenomicEntity, biolink:MolecularEntity, biolink:NamedThing} |
* Uriorcurie |
Entity | |
type: rdf:type of biolink:Association should be fixed at rdf:Statement |
* String |
Entity | |
name: A human-readable name for an attribute or entity. |
0..1 LabelType |
Entity | |
description: a human-readable description of an entity |
0..1 NarrativeText |
Entity | |
has_attribute: connects any entity to an attribute |
* Attribute |
Entity | |
deprecated: A boolean flag indicating that an entity is no longer considered current or valid. |
0..1 Boolean |
Entity | |
has_count: number of things with a particular property |
0..1 Integer |
FrequencyQuantifier | |
has_total: total number of things in a particular reference set |
0..1 Integer |
FrequencyQuantifier | |
has_quotient: None |
0..1 Double |
FrequencyQuantifier | |
has_percentage: equivalent to has quotient multiplied by 100 |
0..1 Double |
FrequencyQuantifier | |
subject_direction_qualifier: Composes with the core concept (+ aspect if provided) to describe a change in its direction or degree. This qualifier qualifies the subject of an association (aka: statement). |
0..1 DirectionQualifierEnum |
EntityToFeatureOrDiseaseQualifiersMixin | |
object_aspect_qualifier: Composes with the core concept to describe new concepts of a different ontological type. e.g. a process in which the core concept participates, a function/activity/role held by the core concept, or a characteristic/quality that inheres in the core concept. The purpose of the aspect slot is to indicate what aspect is being affected in an 'affects' association. This qualifier specifies a change in the object of an association (aka: statement). |
0..1 String |
EntityToFeatureOrDiseaseQualifiersMixin | stability, abundance, expression, exposure |
qualified_predicate: Predicate to be used in an association when subject and object qualifiers are present and the full reading of the statement requires a qualification to the predicate in use in order to refine or increase the specificity of the full statement reading. This qualifier holds a relationship to be used instead of that expressed by the primary predicate, in a ‘full statement’ reading of the association, where qualifier-based semantics are included. This is necessary only in cases where the primary predicate does not work in a full statement reading. |
0..1 String |
EntityToFeatureOrDiseaseQualifiersMixin | |
frequency_qualifier: a qualifier used in a phenotypic association to state how frequent the phenotype is observed in the subject |
0..1 FrequencyValue |
FrequencyQualifierMixin |
LinkML Source
name: gene as a model of disease association
from_schema: https://w3id.org/biolink/biolink-model
is_a: gene to disease association
mixins:
- model to disease association mixin
- entity to disease association mixin
slot_usage:
subject:
name: subject
description: A gene that has a role in modeling the disease. This may be a model
organism ortholog of a known disease gene, or it may be a gene whose mutants
recapitulate core features of the disease.
range: gene or gene product
defining_slots:
- subject
- predicate
- object