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- NCIT_C176008 IAO_0000115 "An autosomal dominant subtype of arrhythmogenic right ventricular dysplasia caused by mutation(s) in the CTNNA3 gene, encoding catenin alpha-3." @default.
- NCIT_C176008 NCIT_NHC0 "C176008" @default.
- NCIT_C176008 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176008 NCIT_P108 "Familial Arrhythmogenic Right Ventricular Dysplasia 13" @default.
- NCIT_C176008 NCIT_P207 "C3810138" @default.
- NCIT_C176008 NCIT_P322 "Cellosaurus" @default.
- NCIT_C176008 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176008 NCIT_R176 NCIT_C200291 @default.
- NCIT_C176008 NCIT_R176 NCIT_C20744 @default.
- NCIT_C176008 NCIT_R176 NCIT_C20745 @default.
- NCIT_C176008 normalizedInformationContent "100" @default.
- NCIT_C176008 referenceCount "1" @default.
- NCIT_C176008 hasExactSynonym "ARVD13" @default.
- NCIT_C176008 hasExactSynonym "Familial Arrhythmogenic Right Ventricular Dysplasia 13" @default.
- NCIT_C176008 inSubset NCIT_C165258 @default.
- NCIT_C176008 inSubset NCIT_C192842 @default.
- NCIT_C176008 type Class @default.
- NCIT_C176008 isDefinedBy ncit.owl @default.
- NCIT_C176008 label "Familial Arrhythmogenic Right Ventricular Dysplasia 13" @default.
- NCIT_C176008 subClassOf Bea2b76ea1475518cb6451f2d76ae8faa @default.
- NCIT_C176008 subClassOf Bf618ba967cba4ba837c51e291016e1ea @default.
- NCIT_C176008 subClassOf NCIT_C176008 @default.
- NCIT_C176008 subClassOf NCIT_C2991 @default.
- NCIT_C176008 subClassOf NCIT_C4873 @default.
- NCIT_C176008 subClassOf NCIT_C53529 @default.
- NCIT_C176008 subClassOf NCIT_C53543 @default.
- NCIT_C176008 subClassOf NCIT_C53547 @default.
- NCIT_C176008 subClassOf NCIT_C7057 @default.
- NCIT_C176008 subClassOf NCIT_C84571 @default.