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Class: DiseaseOrPhenotypicFeatureToEntityAssociationMixin

classDiagram class DiseaseOrPhenotypicFeatureToEntityAssociationMixin DiseaseOrPhenotypicFeatureToEntityAssociationMixin <|-- DiseaseOrPhenotypicFeatureToLocationAssociation DiseaseOrPhenotypicFeatureToEntityAssociationMixin <|-- DiseaseOrPhenotypicFeatureToGeneticInheritanceAssociation DiseaseOrPhenotypicFeatureToEntityAssociationMixin : object DiseaseOrPhenotypicFeatureToEntityAssociationMixin --|> NamedThing : object DiseaseOrPhenotypicFeatureToEntityAssociationMixin : predicate DiseaseOrPhenotypicFeatureToEntityAssociationMixin : subject DiseaseOrPhenotypicFeatureToEntityAssociationMixin --|> DiseaseOrPhenotypicFeature : subject

Slots

Name Cardinality and Range Inheritance Examples
subject:
disease or phenotype 		1
DiseaseOrPhenotypicFeature		 direct MONDO:0017314, MP:0013229
predicate:
Has a value from the Biolink 'related_to' hierarchy. In RDF, this corresponds to rdf:predicate and in Neo4j this corresponds to the relationship type. The convention is for an edge label in snake_case form. For example, biolink:related_to, biolink:causes, biolink:treats 		1
Uriorcurie		 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
NamedThing		 direct

Mixin Usage

mixed into description
DiseaseOrPhenotypicFeatureToLocationAssociation An association between either a disease or a phenotypic feature and an anatomical entity, where the disease/feature manifests in that site.
DiseaseOrPhenotypicFeatureToGeneticInheritanceAssociation An association between either a disease or a phenotypic feature and its mode of (genetic) inheritance.

LinkML Source

name: disease or phenotypic feature to entity association mixin
from_schema: https://w3id.org/biolink/vocab/
mixin: true
slots:
- subject
- predicate
- object
slot_usage:
  subject:
    name: subject
    description: disease or phenotype
    examples:
    - value: MONDO:0017314
      description: Ehlers-Danlos syndrome, vascular type
    - value: MP:0013229
      description: abnormal brain ventricle size
    range: disease or phenotypic feature
defining_slots:
- subject