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- NCIT_C96816 IAO_0000115 "A role used to assert a direct relationship between a disease, disorder or finding and a gene. This restriction can be used when a polymorphism or an abnormality in a gene is either a clinical marker for, a causative event for, or predisposes a subject to a disease. The domain and range for this role are 'Disease, Disorder or Finding' and 'Gene', respectively." @default.
- NCIT_C96816 NCIT_A1 NCIT_C7057 @default.
- NCIT_C96816 NCIT_A2 NCIT_C16612 @default.
- NCIT_C96816 NCIT_NHC0 "C96816" @default.
- NCIT_C96816 NCIT_P106 "Conceptual Entity" @default.
- NCIT_C96816 NCIT_P108 "Disease_Mapped_To_Gene" @default.
- NCIT_C96816 NCIT_P207 "C3273057" @default.
- NCIT_C96816 normalizedInformationContent "100" @default.
- NCIT_C96816 referenceCount "1" @default.
- NCIT_C96816 hasExactSynonym "Disease_Mapped_To_Gene" @default.
- NCIT_C96816 type Class @default.
- NCIT_C96816 isDefinedBy ncit.owl @default.
- NCIT_C96816 label "obsolete Disease_Mapped_To_Gene" @default.
- NCIT_C96816 subClassOf NCIT_C96816 @default.
- NCIT_C96816 subClassOf Thing @default.
- NCIT_C96816 deprecated "true" @default.