GeneAsAModelOfDiseaseAssociation
None
classDiagram
ModelToDiseaseAssociationMixin <|-- GeneAsAModelOfDiseaseAssociation
EntityToDiseaseAssociationMixin <|-- GeneAsAModelOfDiseaseAssociation
GeneToDiseaseAssociation <|-- GeneAsAModelOfDiseaseAssociation
GeneAsAModelOfDiseaseAssociation : aggregator_knowledge_source
GeneAsAModelOfDiseaseAssociation : category
GeneAsAModelOfDiseaseAssociation : description
GeneAsAModelOfDiseaseAssociation : frequency_qualifier
GeneAsAModelOfDiseaseAssociation : has_attribute
GeneAsAModelOfDiseaseAssociation : has_evidence
GeneAsAModelOfDiseaseAssociation : id
GeneAsAModelOfDiseaseAssociation : iri
GeneAsAModelOfDiseaseAssociation : knowledge_source
GeneAsAModelOfDiseaseAssociation : name
GeneAsAModelOfDiseaseAssociation : negated
GeneAsAModelOfDiseaseAssociation : object
GeneAsAModelOfDiseaseAssociation : onset_qualifier
GeneAsAModelOfDiseaseAssociation : original_knowledge_source
GeneAsAModelOfDiseaseAssociation : predicate
GeneAsAModelOfDiseaseAssociation : primary_knowledge_source
GeneAsAModelOfDiseaseAssociation : publications
GeneAsAModelOfDiseaseAssociation : qualifiers
GeneAsAModelOfDiseaseAssociation : severity_qualifier
GeneAsAModelOfDiseaseAssociation : source
GeneAsAModelOfDiseaseAssociation : subject
GeneAsAModelOfDiseaseAssociation : timepoint
GeneAsAModelOfDiseaseAssociation : type
Parent Classes
- Entity
- Association
- GeneToDiseaseAssociation [ entity to disease association mixin gene to entity association mixin]
- GeneAsAModelOfDiseaseAssociation [ model to disease association mixin entity to disease association mixin]
- GeneToDiseaseAssociation [ entity to disease association mixin gene to entity association mixin]
- Association
Slots
Name | Description |
---|---|
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. |
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 , etc. 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} |
description | a human-readable description of an entity |
frequency_qualifier | a qualifier used in a phenotypic association to state how frequent the phenotype is observed in the subject |
has_attribute | connects any entity to an attribute |
has_evidence | connects an association to an instance of supporting evidence |
id | A unique identifier for an entity. Must be either a CURIE shorthand for a URI or a complete URI |
iri | An IRI for an entity. This is determined by the id using expansion rules. |
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. |
name | A human-readable name for an attribute or entity. |
negated | if set to true, then the association is negated i.e. is not true |
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. |
onset_qualifier | a qualifier used in a phenotypic association to state when the phenotype appears is in the subject |
original_knowledge_source | None |
predicate | A high-level grouping for the relationship type. AKA minimal predicate. This is analogous to category for nodes. |
primary_knowledge_source | The most upstream source of the knowledge expressed in an Association that an implementer can identify (may or may not be the 'original' source). |
publications | connects an association to publications supporting the association |
qualifiers | connects an association to qualifiers that modify or qualify the meaning of that association |
severity_qualifier | a qualifier used in a phenotypic association to state how severe the phenotype is in the subject |
source | None |
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. |
timepoint | a point in time |
type | None |
Mappings
Mapping Type | Mapped Value |
---|---|
self | ['biolink:GeneAsAModelOfDiseaseAssociation'] |
native | ['biolink:GeneAsAModelOfDiseaseAssociation'] |