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- NCIT_R38 IAO_0000115 "A role used to indicate that molecular abnormalities in a gene may be associated with the manifestation of a disease. The role is used to assert a link between a gene and a disease when the association is considered to have clinical relevance. The domain and range for this role are 'Gene' and 'Disease, Disorder or Finding', respectively." @default.
- NCIT_R38 NCIT_NHC0 "R38" @default.
- NCIT_R38 NCIT_P106 "Conceptual Entity" @default.
- NCIT_R38 NCIT_P107 "Associated With Disease" @default.
- NCIT_R38 NCIT_P108 "Gene_Associated_With_Disease" @default.
- NCIT_R38 hasExactSynonym "Gene_Associated_With_Disease" @default.
- NCIT_R38 type ObjectProperty @default.
- NCIT_R38 domain NCIT_C16612 @default.
- NCIT_R38 isDefinedBy ncit.owl @default.
- NCIT_R38 label "Gene_Associated_With_Disease" @default.
- NCIT_R38 range NCIT_C7057 @default.
- NCIT_R38 category gene_associated_with_condition @default.
- NCIT_R38 category genetic_association @default.
- NCIT_R38 category related_to @default.
- NCIT_R38 category related_to_at_instance_level @default.