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- NCIT_C126872 IAO_0000115 "A congenital disorder of glycosylation sub-type caused by mutation(s) in the MPDU1 gene, encoding mannose-P-dolichol utilization defect 1 protein." @default.
- NCIT_C126872 NCIT_NHC0 "C126872" @default.
- NCIT_C126872 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C126872 NCIT_P108 "Congenital Disorder of Glycosylation Type If" @default.
- NCIT_C126872 NCIT_P207 "C1836669" @default.
- NCIT_C126872 NCIT_P322 "Cellosaurus" @default.
- NCIT_C126872 NCIT_R176 NCIT_C16612 @default.
- NCIT_C126872 NCIT_R176 NCIT_C191660 @default.
- NCIT_C126872 NCIT_R176 NCIT_C20194 @default.
- NCIT_C126872 normalizedInformationContent "100" @default.
- NCIT_C126872 referenceCount "1" @default.
- NCIT_C126872 hasExactSynonym "CDGIf" @default.
- NCIT_C126872 hasExactSynonym "Congenital Disorder of Glycosylation Type If" @default.
- NCIT_C126872 inSubset NCIT_C165258 @default.
- NCIT_C126872 inSubset NCIT_C192842 @default.
- NCIT_C126872 type Class @default.
- NCIT_C126872 isDefinedBy ncit.owl @default.
- NCIT_C126872 label "Congenital Disorder of Glycosylation Type If" @default.
- NCIT_C126872 subClassOf B5534fe0e7db937136e0c27adcb493d6c @default.
- NCIT_C126872 subClassOf B8f960b67710990e00beb3d0afde9c76e @default.
- NCIT_C126872 subClassOf NCIT_C126872 @default.
- NCIT_C126872 subClassOf NCIT_C28193 @default.
- NCIT_C126872 subClassOf NCIT_C2991 @default.
- NCIT_C126872 subClassOf NCIT_C3235 @default.
- NCIT_C126872 subClassOf NCIT_C4873 @default.
- NCIT_C126872 subClassOf NCIT_C53529 @default.
- NCIT_C126872 subClassOf NCIT_C53543 @default.
- NCIT_C126872 subClassOf NCIT_C53547 @default.
- NCIT_C126872 subClassOf NCIT_C7057 @default.
- NCIT_C126872 subClassOf NCIT_C84615 @default.
- NCIT_C126872 subClassOf NCIT_C97089 @default.