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Class: ClinicalModifier

Description: Used to characterize and specify the phenotypic abnormalities defined in the phenotypic abnormality sub-ontology, with respect to severity, laterality, and other aspects
classDiagram class ClinicalModifier ClinicalAttribute <|-- ClinicalModifier ClinicalModifier : category ClinicalModifier : deprecated ClinicalModifier : description ClinicalModifier : full_name ClinicalModifier : has_attribute ClinicalModifier --|> Attribute : has_attribute ClinicalModifier : has_attribute_type ClinicalModifier --|> OntologyClass : has_attribute_type ClinicalModifier : has_qualitative_value ClinicalModifier --|> NamedThing : has_qualitative_value ClinicalModifier : has_quantitative_value ClinicalModifier --|> QuantityValue : has_quantitative_value ClinicalModifier : id ClinicalModifier : iri ClinicalModifier : name ClinicalModifier : provided_by ClinicalModifier : synonym ClinicalModifier : type ClinicalModifier : xref

Inheritance

Slots

Name Cardinality and Range Inheritance Examples
name:
The human-readable 'attribute name' can be set to a string which reflects its context of interpretation, e.g. SEPIO evidence/provenance/confidence annotation or it can default to the name associated with the 'has attribute type' slot ontology term.
0..1
LabelType
Entity, Attribute
has_attribute_type:
connects an attribute to a class that describes it
1..1
OntologyClass
Attribute
has_quantitative_value:
connects an attribute to a value
0..*
QuantityValue
Attribute
has_qualitative_value:
connects an attribute to a value
0..1
NamedThing
Attribute
iri:
An IRI for an entity. This is determined by the id using expansion rules.
0..1
IriType
Entity, Attribute
id:
A unique identifier for an entity. Must be either a CURIE shorthand for a URI or a complete URI
1..1
String
OntologyClass, Entity
provided_by:
The value in this node property represents the knowledge provider that created or assembled the node and all of its attributes. Used internally to represent how a particular node made its way into a knowledge provider or graph.
0..*
String
NamedThing
xref:
A database cross reference or alternative identifier for a NamedThing or edge between two NamedThings. This property should point to a database record or webpage that supports the existence of the edge, or gives more detail about the edge. This property can be used on a node or edge to provide multiple URIs or CURIE cross references.
0..*
Uriorcurie
NamedThing
full_name:
a long-form human readable name for a thing
0..1
LabelType
NamedThing
synonym:
Alternate human-readable names for a thing
0..*
LabelType
NamedThing
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}
1..*
Uriorcurie
Entity
type:
None
0..*
String
Entity
description:
a human-readable description of an entity
0..1
NarrativeText
Entity
has_attribute:
connects any entity to an attribute
0..*
Attribute
Entity
deprecated:
A boolean flag indicating that an entity is no longer considered current or valid.
0..1
Boolean
Entity

LinkML Source

name: clinical modifier
description: Used to characterize and specify the phenotypic abnormalities defined
  in the phenotypic abnormality sub-ontology, with respect to severity, laterality,
  and other aspects
from_schema: https://w3id.org/biolink/biolink-model
is_a: clinical attribute