Class: EntityToPhenotypicFeatureAssociationMixin
classDiagram
class EntityToPhenotypicFeatureAssociationMixin
FrequencyQuantifier <|-- EntityToPhenotypicFeatureAssociationMixin
EntityToFeatureOrDiseaseQualifiersMixin <|-- EntityToPhenotypicFeatureAssociationMixin
EntityToPhenotypicFeatureAssociationMixin <|-- PhenotypicFeatureToPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- GenotypeToPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- ExposureEventToPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- DiseaseToPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- CaseToPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- BehaviorToBehavioralFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- GeneToDiseaseOrPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- GeneToPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin <|-- VariantToPhenotypicFeatureAssociation
EntityToPhenotypicFeatureAssociationMixin : anatomical_context_qualifier
EntityToPhenotypicFeatureAssociationMixin : disease_context_qualifier
EntityToPhenotypicFeatureAssociationMixin --|> Disease : disease_context_qualifier
EntityToPhenotypicFeatureAssociationMixin : frequency_qualifier
EntityToPhenotypicFeatureAssociationMixin : has_count
EntityToPhenotypicFeatureAssociationMixin : has_percentage
EntityToPhenotypicFeatureAssociationMixin : has_quotient
EntityToPhenotypicFeatureAssociationMixin : has_total
EntityToPhenotypicFeatureAssociationMixin : object
EntityToPhenotypicFeatureAssociationMixin --|> PhenotypicFeature : object
EntityToPhenotypicFeatureAssociationMixin : object_aspect_qualifier
EntityToPhenotypicFeatureAssociationMixin : object_direction_qualifier
EntityToPhenotypicFeatureAssociationMixin --|> DirectionQualifierEnum : object_direction_qualifier
EntityToPhenotypicFeatureAssociationMixin : object_specialization_qualifier
EntityToPhenotypicFeatureAssociationMixin : predicate
EntityToPhenotypicFeatureAssociationMixin : qualified_predicate
EntityToPhenotypicFeatureAssociationMixin : sex_qualifier
EntityToPhenotypicFeatureAssociationMixin --|> BiologicalSex : sex_qualifier
EntityToPhenotypicFeatureAssociationMixin : subject
EntityToPhenotypicFeatureAssociationMixin --|> NamedThing : subject
EntityToPhenotypicFeatureAssociationMixin : subject_aspect_qualifier
EntityToPhenotypicFeatureAssociationMixin : subject_direction_qualifier
EntityToPhenotypicFeatureAssociationMixin --|> DirectionQualifierEnum : subject_direction_qualifier
EntityToPhenotypicFeatureAssociationMixin : subject_specialization_qualifier
Inheritance
- FrequencyQualifierMixin
- EntityToFeatureOrDiseaseQualifiersMixin
- EntityToPhenotypicFeatureAssociationMixin [ FrequencyQuantifier]
- EntityToFeatureOrDiseaseQualifiersMixin
Slots
Name | Cardinality and Range | Inheritance | Examples |
---|---|---|---|
subject: connects an association to the subject of the association. For example, in a gene-to-phenotype association, the gene is subject and phenotype is object. |
1 NamedThing |
direct | |
predicate: A high-level grouping for the relationship type. AKA minimal predicate. This is analogous to category for nodes. |
1 PredicateType |
direct | |
object: connects an association to the object of the association. For example, in a gene-to-phenotype association, the gene is subject and phenotype is object. |
1 PhenotypicFeature |
direct | HP:0002487, WBPhenotype:0000180, MP:0001569 |
sex_qualifier: a qualifier used in a phenotypic association to state whether the association is specific to a particular sex. |
0..1 BiologicalSex |
direct | |
disease_context_qualifier: A context qualifier representing a disease or condition in which a relationship expressed in an association took place. |
0..1 Disease |
direct | 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 |
direct | |
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 |
direct | |
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 |
direct | blood, cerebral cortext |
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_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 String |
EntityToFeatureOrDiseaseQualifiersMixin | stability, abundance, expression, exposure |
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 |
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 |
EntityToFeatureOrDiseaseQualifiersMixin | |
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 |
Mixin Usage
mixed into | description |
---|---|
PhenotypicFeatureToPhenotypicFeatureAssociation | Association between two concept nodes of phenotypic character, qualified by the predicate used. This association may typically be used to specify 'similar_to' or 'member_of' relationships. |
GenotypeToPhenotypicFeatureAssociation | Any association between one genotype and a phenotypic feature, where having the genotype confers the phenotype, either in isolation or through environment |
ExposureEventToPhenotypicFeatureAssociation | Any association between an environment and a phenotypic feature, where being in the environment influences the phenotype. |
DiseaseToPhenotypicFeatureAssociation | An association between a disease and a phenotypic feature in which the phenotypic feature is associated with the disease in some way. |
CaseToPhenotypicFeatureAssociation | An association between a case (e.g. individual patient) and a phenotypic feature in which the individual has or has had the phenotype. |
BehaviorToBehavioralFeatureAssociation | An association between an mixture behavior and a behavioral feature manifested by the individual exhibited or has exhibited the behavior. |
GeneToDiseaseOrPhenotypicFeatureAssociation | None |
GeneToPhenotypicFeatureAssociation | None |
VariantToPhenotypicFeatureAssociation | None |
LinkML Source
name: entity to phenotypic feature association mixin
from_schema: https://w3id.org/biolink/biolink-model
is_a: entity to feature or disease qualifiers mixin
mixin: true
mixins:
- frequency quantifier
slots:
- subject
- predicate
- object
- sex qualifier
- disease context qualifier
- subject specialization qualifier
- object specialization qualifier
- anatomical context qualifier
slot_usage:
object:
name: object
examples:
- value: HP:0002487
description: Hyperkinesis
- value: WBPhenotype:0000180
description: axon morphology variant
- value: MP:0001569
description: abnormal circulating bilirubin level
values_from:
- upheno
- hp
- mp
- wbphenotype
range: phenotypic feature
defining_slots:
- subject
- predicate
- object