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- NCIT_C179473 IAO_0000115 "An inherited condition caused by mutation(s) in the MET gene, encoding hepatocyte growth factor receptor. The condition is characterized by an increased risk of developing papillary renal cell carcinoma." @default.
- NCIT_C179473 NCIT_A13 NCIT_C18325 @default.
- NCIT_C179473 NCIT_NHC0 "C179473" @default.
- NCIT_C179473 NCIT_P106 "Finding" @default.
- NCIT_C179473 NCIT_P108 "Genetic Predisposition to Papillary Renal Cell Carcinoma" @default.
- NCIT_C179473 NCIT_P208 "CL1662270" @default.
- NCIT_C179473 NCIT_P322 "CCPS" @default.
- NCIT_C179473 normalizedInformationContent "100" @default.
- NCIT_C179473 referenceCount "1" @default.
- NCIT_C179473 hasExactSynonym "Genetic Predisposition to Papillary Renal Cell Carcinoma" @default.
- NCIT_C179473 inSubset NCIT_C177281 @default.
- NCIT_C179473 inSubset NCIT_C177516 @default.
- NCIT_C179473 type Class @default.
- NCIT_C179473 isDefinedBy ncit.owl @default.
- NCIT_C179473 label "Genetic Predisposition to Papillary Renal Cell Carcinoma" @default.
- NCIT_C179473 subClassOf NCIT_C171210 @default.
- NCIT_C179473 subClassOf NCIT_C178391 @default.
- NCIT_C179473 subClassOf NCIT_C179473 @default.
- NCIT_C179473 subClassOf NCIT_C3367 @default.
- NCIT_C179473 subClassOf NCIT_C36291 @default.
- NCIT_C179473 subClassOf NCIT_C7057 @default.