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- NCIT_C177248 IAO_0000115 "An autosomal dominant subtype of arrhythmogenic right ventricular dysplasia caused by mutation(s) in the DSG2 gene, encoding desmoglein-2." @default.
- NCIT_C177248 NCIT_NHC0 "C177248" @default.
- NCIT_C177248 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C177248 NCIT_P108 "Familial Arrhythmogenic Right Ventricular Dysplasia 10" @default.
- NCIT_C177248 NCIT_P207 "C1857777" @default.
- NCIT_C177248 NCIT_P322 "Cellosaurus" @default.
- NCIT_C177248 NCIT_R176 NCIT_C16612 @default.
- NCIT_C177248 NCIT_R176 NCIT_C177647 @default.
- NCIT_C177248 NCIT_R176 NCIT_C20744 @default.
- NCIT_C177248 normalizedInformationContent "100" @default.
- NCIT_C177248 referenceCount "1" @default.
- NCIT_C177248 hasExactSynonym "ARVD10" @default.
- NCIT_C177248 hasExactSynonym "Familial Arrhythmogenic Right Ventricular Dysplasia 10" @default.
- NCIT_C177248 inSubset NCIT_C165258 @default.
- NCIT_C177248 inSubset NCIT_C192842 @default.
- NCIT_C177248 type Class @default.
- NCIT_C177248 isDefinedBy ncit.owl @default.
- NCIT_C177248 label "Familial Arrhythmogenic Right Ventricular Dysplasia 10" @default.
- NCIT_C177248 subClassOf B70ce0ab31d91820d63afdfb7db0cf516 @default.
- NCIT_C177248 subClassOf Bee7f2d106060c696ba0fec45933ad10a @default.
- NCIT_C177248 subClassOf NCIT_C177248 @default.
- NCIT_C177248 subClassOf NCIT_C2991 @default.
- NCIT_C177248 subClassOf NCIT_C4873 @default.
- NCIT_C177248 subClassOf NCIT_C53529 @default.
- NCIT_C177248 subClassOf NCIT_C53543 @default.
- NCIT_C177248 subClassOf NCIT_C53547 @default.
- NCIT_C177248 subClassOf NCIT_C7057 @default.
- NCIT_C177248 subClassOf NCIT_C84571 @default.