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- NCIT_C124841 IAO_0000115 "A rare, autosomal recessive syndrome characterized by orofacial anomalies, metacarpal abnormalities with central polydactyly, and cerebellar dysgenesis." @default.
- NCIT_C124841 NCIT_NHC0 "C124841" @default.
- NCIT_C124841 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C124841 NCIT_P108 "Orofaciodigital Syndrome Type 6" @default.
- NCIT_C124841 NCIT_P207 "C2745997" @default.
- NCIT_C124841 NCIT_P322 "Cellosaurus" @default.
- NCIT_C124841 NCIT_R176 NCIT_C16612 @default.
- NCIT_C124841 NCIT_R176 NCIT_C200266 @default.
- NCIT_C124841 NCIT_R176 NCIT_C20194 @default.
- NCIT_C124841 normalizedInformationContent "100" @default.
- NCIT_C124841 referenceCount "1" @default.
- NCIT_C124841 hasExactSynonym "Orofaciodigital Syndrome Type 6" @default.
- NCIT_C124841 hasExactSynonym "Varadi-Papp Syndrome" @default.
- NCIT_C124841 inSubset NCIT_C165258 @default.
- NCIT_C124841 inSubset NCIT_C192842 @default.
- NCIT_C124841 type Class @default.
- NCIT_C124841 isDefinedBy ncit.owl @default.
- NCIT_C124841 label "Orofaciodigital Syndrome Type 6" @default.
- NCIT_C124841 subClassOf B441dc02797754e1fb52f8925799f1e00 @default.
- NCIT_C124841 subClassOf B90f604d6c6adb16b9584ca0967476f9e @default.
- NCIT_C124841 subClassOf NCIT_C124841 @default.
- NCIT_C124841 subClassOf NCIT_C28193 @default.
- NCIT_C124841 subClassOf NCIT_C2991 @default.
- NCIT_C124841 subClassOf NCIT_C4873 @default.
- NCIT_C124841 subClassOf NCIT_C53529 @default.
- NCIT_C124841 subClassOf NCIT_C53543 @default.
- NCIT_C124841 subClassOf NCIT_C53547 @default.
- NCIT_C124841 subClassOf NCIT_C7057 @default.