Class: GeneToPhenotypicFeatureAssociation

classDiagram class GeneToPhenotypicFeatureAssociation EntityToPhenotypicFeatureAssociationMixin <|-- GeneToPhenotypicFeatureAssociation GeneToEntityAssociationMixin <|-- GeneToPhenotypicFeatureAssociation GeneToDiseaseOrPhenotypicFeatureAssociation <|-- GeneToPhenotypicFeatureAssociation GeneToPhenotypicFeatureAssociation : aggregator_knowledge_source GeneToPhenotypicFeatureAssociation : category GeneToPhenotypicFeatureAssociation : description GeneToPhenotypicFeatureAssociation : frequency_qualifier GeneToPhenotypicFeatureAssociation : has_attribute GeneToPhenotypicFeatureAssociation --|> attribute : has_attribute GeneToPhenotypicFeatureAssociation : has_count GeneToPhenotypicFeatureAssociation : has_evidence GeneToPhenotypicFeatureAssociation --|> evidence type : has_evidence GeneToPhenotypicFeatureAssociation : has_percentage GeneToPhenotypicFeatureAssociation : has_quotient GeneToPhenotypicFeatureAssociation : has_total GeneToPhenotypicFeatureAssociation : id GeneToPhenotypicFeatureAssociation : iri GeneToPhenotypicFeatureAssociation : knowledge_source GeneToPhenotypicFeatureAssociation : name GeneToPhenotypicFeatureAssociation : negated GeneToPhenotypicFeatureAssociation : object GeneToPhenotypicFeatureAssociation --|> phenotypic feature : object GeneToPhenotypicFeatureAssociation : object_category GeneToPhenotypicFeatureAssociation --|> ontology class : object_category GeneToPhenotypicFeatureAssociation : object_category_closure GeneToPhenotypicFeatureAssociation --|> ontology class : object_category_closure GeneToPhenotypicFeatureAssociation : object_closure GeneToPhenotypicFeatureAssociation : object_direction_qualifier GeneToPhenotypicFeatureAssociation --|> DirectionQualifierEnum : object_direction_qualifier GeneToPhenotypicFeatureAssociation : object_label_closure GeneToPhenotypicFeatureAssociation : object_namespace GeneToPhenotypicFeatureAssociation : onset_qualifier GeneToPhenotypicFeatureAssociation --|> onset : onset_qualifier GeneToPhenotypicFeatureAssociation : original_object GeneToPhenotypicFeatureAssociation : original_predicate GeneToPhenotypicFeatureAssociation : original_subject GeneToPhenotypicFeatureAssociation : predicate GeneToPhenotypicFeatureAssociation : primary_knowledge_source GeneToPhenotypicFeatureAssociation : publications GeneToPhenotypicFeatureAssociation --|> publication : publications GeneToPhenotypicFeatureAssociation : qualifiers GeneToPhenotypicFeatureAssociation --|> ontology class : qualifiers GeneToPhenotypicFeatureAssociation : retrieval_source_ids GeneToPhenotypicFeatureAssociation --|> retrieval source : retrieval_source_ids GeneToPhenotypicFeatureAssociation : severity_qualifier GeneToPhenotypicFeatureAssociation --|> severity value : severity_qualifier GeneToPhenotypicFeatureAssociation : sex_qualifier GeneToPhenotypicFeatureAssociation --|> biological sex : sex_qualifier GeneToPhenotypicFeatureAssociation : subject GeneToPhenotypicFeatureAssociation --|> gene or gene product : subject GeneToPhenotypicFeatureAssociation : subject_aspect_qualifier GeneToPhenotypicFeatureAssociation --|> GeneOrGeneProductOrChemicalEntityAspectEnum : subject_aspect_qualifier GeneToPhenotypicFeatureAssociation : subject_category GeneToPhenotypicFeatureAssociation --|> ontology class : subject_category GeneToPhenotypicFeatureAssociation : subject_category_closure GeneToPhenotypicFeatureAssociation --|> ontology class : subject_category_closure GeneToPhenotypicFeatureAssociation : subject_closure GeneToPhenotypicFeatureAssociation : subject_label_closure GeneToPhenotypicFeatureAssociation : subject_namespace GeneToPhenotypicFeatureAssociation : timepoint GeneToPhenotypicFeatureAssociation : type

name: gene to phenotypic feature association
from_schema: https://w3id.org/biolink/biolink-model
exact_mappings:
- WBVocab:Gene-Phenotype-Association
is_a: gene to disease or phenotypic feature association
mixins:
- entity to phenotypic feature association mixin
- gene to entity association mixin
slot_usage:
  subject:
    name: subject
    description: gene in which variation is correlated with the phenotypic feature
    examples:
    - value: HGNC:2197
      description: COL1A1 (Human)
    domain_of:
    - association
    range: gene or gene product
  object:
    name: object
    domain_of:
    - association
    range: phenotypic feature
defining_slots:
- subject
- object