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- NCIT_C84693 IAO_0000115 "A genetic skin disorder caused by mutations in the KRT9 gene. It is characterized by hyperkeratosis in the palms and soles resulting in abnormal thickening of the skin in these areas." @default.
- NCIT_C84693 NCIT_NHC0 "C84693" @default.
- NCIT_C84693 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84693 NCIT_P108 "Epidermolytic Palmoplantar Keratoderma" @default.
- NCIT_C84693 NCIT_P207 "C1721006" @default.
- NCIT_C84693 NCIT_R100 NCIT_C12219 @default.
- NCIT_C84693 NCIT_R100 NCIT_C12907 @default.
- NCIT_C84693 NCIT_R100 NCIT_C12919 @default.
- NCIT_C84693 NCIT_R101 NCIT_C12219 @default.
- NCIT_C84693 NCIT_R101 NCIT_C12470 @default.
- NCIT_C84693 NCIT_R101 NCIT_C13018 @default.
- NCIT_C84693 NCIT_R108 NCIT_C3367 @default.
- NCIT_C84693 NCIT_R108 NCIT_C36278 @default.
- NCIT_C84693 NCIT_R108 NCIT_C36281 @default.
- NCIT_C84693 NCIT_R108 NCIT_C39570 @default.
- NCIT_C84693 NCIT_R108 NCIT_C7057 @default.
- NCIT_C84693 normalizedInformationContent "100" @default.
- NCIT_C84693 referenceCount "1" @default.
- NCIT_C84693 hasExactSynonym "Epidermolytic Palmoplantar Keratoderma" @default.
- NCIT_C84693 type Class @default.
- NCIT_C84693 isDefinedBy ncit.owl @default.
- NCIT_C84693 label "Epidermolytic Palmoplantar Keratoderma" @default.
- NCIT_C84693 subClassOf B1339a4a9b2f5d083ed9a58eacf2613d2 @default.
- NCIT_C84693 subClassOf B9e2293b8fa3cf7487b34d284e11c14cf @default.
- NCIT_C84693 subClassOf NCIT_C27551 @default.
- NCIT_C84693 subClassOf NCIT_C27555 @default.
- NCIT_C84693 subClassOf NCIT_C2991 @default.
- NCIT_C84693 subClassOf NCIT_C3371 @default.
- NCIT_C84693 subClassOf NCIT_C34745 @default.
- NCIT_C84693 subClassOf NCIT_C34748 @default.
- NCIT_C84693 subClassOf NCIT_C53529 @default.
- NCIT_C84693 subClassOf NCIT_C53531 @default.
- NCIT_C84693 subClassOf NCIT_C7057 @default.
- NCIT_C84693 subClassOf NCIT_C84693 @default.