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- NCIT_C128191 IAO_0000115 "An autosomal dominant genetic disorder caused by mutation(s) in the FOXC2 gene, encoding forkhead box protein C2. The condition is characterized by lymphedema and distichiasis." @default.
- NCIT_C128191 NCIT_NHC0 "C128191" @default.
- NCIT_C128191 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C128191 NCIT_P108 "Lymphedema-Distichiasis Syndrome" @default.
- NCIT_C128191 NCIT_P207 "C0265345" @default.
- NCIT_C128191 NCIT_P322 "Cellosaurus" @default.
- NCIT_C128191 NCIT_R176 NCIT_C16612 @default.
- NCIT_C128191 NCIT_R176 NCIT_C20420 @default.
- NCIT_C128191 NCIT_R176 NCIT_C48218 @default.
- NCIT_C128191 NCIT_R176 NCIT_C54362 @default.
- NCIT_C128191 normalizedInformationContent "100" @default.
- NCIT_C128191 referenceCount "1" @default.
- NCIT_C128191 hasExactSynonym "Lymphedema-Distichiasis Syndrome" @default.
- NCIT_C128191 inSubset NCIT_C165258 @default.
- NCIT_C128191 inSubset NCIT_C192842 @default.
- NCIT_C128191 type Class @default.
- NCIT_C128191 isDefinedBy ncit.owl @default.
- NCIT_C128191 label "Lymphedema-Distichiasis Syndrome" @default.
- NCIT_C128191 subClassOf B279e0ac3292e8b89d56144d4e1e08df8 @default.
- NCIT_C128191 subClassOf Ba8487cc4440f6fc3043748b931e511e0 @default.
- NCIT_C128191 subClassOf NCIT_C128191 @default.
- NCIT_C128191 subClassOf NCIT_C28193 @default.
- NCIT_C128191 subClassOf NCIT_C2991 @default.
- NCIT_C128191 subClassOf NCIT_C7057 @default.