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- NCIT_C179470 IAO_0000115 "An inherited condition caused by mutation(s) in the NOTCH3 or PDGFRB genes, encoding neurogenic locus notch homolog protein 3 and platelet-derived growth factor receptor beta, respectively. The condition is characterized by an increased risk of developing myofibroma." @default.
- NCIT_C179470 NCIT_A13 NCIT_C106436 @default.
- NCIT_C179470 NCIT_A13 NCIT_C24667 @default.
- NCIT_C179470 NCIT_NHC0 "C179470" @default.
- NCIT_C179470 NCIT_P106 "Finding" @default.
- NCIT_C179470 NCIT_P108 "Genetic Predisposition to Myofibromatosis" @default.
- NCIT_C179470 NCIT_P208 "CL1662289" @default.
- NCIT_C179470 NCIT_P322 "CCPS" @default.
- NCIT_C179470 normalizedInformationContent "100" @default.
- NCIT_C179470 referenceCount "1" @default.
- NCIT_C179470 hasExactSynonym "Genetic Predisposition to Myofibromatosis" @default.
- NCIT_C179470 inSubset NCIT_C177281 @default.
- NCIT_C179470 inSubset NCIT_C177516 @default.
- NCIT_C179470 type Class @default.
- NCIT_C179470 isDefinedBy ncit.owl @default.
- NCIT_C179470 label "Genetic Predisposition to Myofibromatosis" @default.
- NCIT_C179470 subClassOf NCIT_C178391 @default.
- NCIT_C179470 subClassOf NCIT_C179470 @default.
- NCIT_C179470 subClassOf NCIT_C3367 @default.
- NCIT_C179470 subClassOf NCIT_C36291 @default.
- NCIT_C179470 subClassOf NCIT_C7057 @default.