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- NCIT_C173471 IAO_0000115 "An autosomal dominant arrhythmogenic cardiomyopathy caused by mutations(s) in the PKP2 gene on chromosome 12p11, encoding plakophilin 2. It is characterized by right ventricular structural abnormalities and arrhythmias, electrocardiographic depolarization/repolarization changes, and sudden death." @default.
- NCIT_C173471 NCIT_NHC0 "C173471" @default.
- NCIT_C173471 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C173471 NCIT_P108 "Familial Arrhythmogenic Right Ventricular Dysplasia 9" @default.
- NCIT_C173471 NCIT_P207 "C1836906" @default.
- NCIT_C173471 NCIT_P322 "Cellosaurus" @default.
- NCIT_C173471 NCIT_R176 NCIT_C16612 @default.
- NCIT_C173471 NCIT_R176 NCIT_C173497 @default.
- NCIT_C173471 NCIT_R176 NCIT_C20988 @default.
- NCIT_C173471 NCIT_R176 NCIT_C21295 @default.
- NCIT_C173471 normalizedInformationContent "100" @default.
- NCIT_C173471 referenceCount "1" @default.
- NCIT_C173471 hasExactSynonym "ARVD9" @default.
- NCIT_C173471 hasExactSynonym "Familial Arrhythmogenic Right Ventricular Dysplasia 9" @default.
- NCIT_C173471 inSubset NCIT_C165258 @default.
- NCIT_C173471 inSubset NCIT_C192842 @default.
- NCIT_C173471 type Class @default.
- NCIT_C173471 isDefinedBy ncit.owl @default.
- NCIT_C173471 label "Familial Arrhythmogenic Right Ventricular Dysplasia 9" @default.
- NCIT_C173471 subClassOf B78fa3ea5c3048bfba220826df1d90ee0 @default.
- NCIT_C173471 subClassOf Ba52f5af7e3132fa987a9f05ee49568cb @default.
- NCIT_C173471 subClassOf NCIT_C173471 @default.
- NCIT_C173471 subClassOf NCIT_C2991 @default.
- NCIT_C173471 subClassOf NCIT_C4873 @default.
- NCIT_C173471 subClassOf NCIT_C53529 @default.
- NCIT_C173471 subClassOf NCIT_C53543 @default.
- NCIT_C173471 subClassOf NCIT_C53547 @default.
- NCIT_C173471 subClassOf NCIT_C7057 @default.
- NCIT_C173471 subClassOf NCIT_C84571 @default.