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- NCIT_C85009 IAO_0000115 "A rare, autosomal dominant disorder caused usually by mutations in the KIT gene. It is characterized by abnormalities in the development of melanocytes. It presents with multiple symmetrical hypopigmented or depigmented patches of skin and a midline patch of white hair." @default.
- NCIT_C85009 NCIT_NHC0 "C85009" @default.
- NCIT_C85009 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C85009 NCIT_P108 "Piebaldism" @default.
- NCIT_C85009 NCIT_P207 "C0080024" @default.
- NCIT_C85009 NCIT_R176 NCIT_C16612 @default.
- NCIT_C85009 NCIT_R176 NCIT_C18609 @default.
- NCIT_C85009 NCIT_R176 NCIT_C20103 @default.
- NCIT_C85009 NCIT_R176 NCIT_C20719 @default.
- NCIT_C85009 NCIT_R176 NCIT_C21281 @default.
- NCIT_C85009 NCIT_R176 NCIT_C21295 @default.
- NCIT_C85009 NCIT_R176 NCIT_C25870 @default.
- NCIT_C85009 NCIT_R176 NCIT_C25871 @default.
- NCIT_C85009 NCIT_R176 NCIT_C25872 @default.
- NCIT_C85009 normalizedInformationContent "100" @default.
- NCIT_C85009 referenceCount "1" @default.
- NCIT_C85009 hasExactSynonym "Piebaldism" @default.
- NCIT_C85009 type Class @default.
- NCIT_C85009 isDefinedBy ncit.owl @default.
- NCIT_C85009 label "Piebaldism" @default.
- NCIT_C85009 subClassOf B940caf576fd9479ff7d9ebbdce93d1c0 @default.
- NCIT_C85009 subClassOf Bd12fb60cab05d0a41bb52eaf90449955 @default.
- NCIT_C85009 subClassOf NCIT_C2991 @default.
- NCIT_C85009 subClassOf NCIT_C4873 @default.
- NCIT_C85009 subClassOf NCIT_C53529 @default.
- NCIT_C85009 subClassOf NCIT_C53543 @default.
- NCIT_C85009 subClassOf NCIT_C53547 @default.
- NCIT_C85009 subClassOf NCIT_C7057 @default.
- NCIT_C85009 subClassOf NCIT_C85009 @default.