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- NCIT_C126870 IAO_0000115 "A congenital disorder of glycosylation sub-type caused by mutation(s) in the ALG3 gene, encoding dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase." @default.
- NCIT_C126870 NCIT_NHC0 "C126870" @default.
- NCIT_C126870 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C126870 NCIT_P108 "Congenital Disorder of Glycosylation Type Id" @default.
- NCIT_C126870 NCIT_P207 "C1832736" @default.
- NCIT_C126870 NCIT_P322 "Cellosaurus" @default.
- NCIT_C126870 NCIT_R176 NCIT_C16612 @default.
- NCIT_C126870 NCIT_R176 NCIT_C191650 @default.
- NCIT_C126870 NCIT_R176 NCIT_C21281 @default.
- NCIT_C126870 NCIT_R176 NCIT_C25870 @default.
- NCIT_C126870 NCIT_R176 NCIT_C26147 @default.
- NCIT_C126870 normalizedInformationContent "100" @default.
- NCIT_C126870 referenceCount "1" @default.
- NCIT_C126870 hasExactSynonym "CDGId" @default.
- NCIT_C126870 hasExactSynonym "Congenital Disorder of Glycosylation Type Id" @default.
- NCIT_C126870 inSubset NCIT_C165258 @default.
- NCIT_C126870 inSubset NCIT_C192842 @default.
- NCIT_C126870 type Class @default.
- NCIT_C126870 isDefinedBy ncit.owl @default.
- NCIT_C126870 label "Congenital Disorder of Glycosylation Type Id" @default.
- NCIT_C126870 subClassOf B81e56de5d5db02c8e9feada75f1175a2 @default.
- NCIT_C126870 subClassOf Bb791e58eef5eb495d793059498432aa4 @default.
- NCIT_C126870 subClassOf NCIT_C126870 @default.
- NCIT_C126870 subClassOf NCIT_C28193 @default.
- NCIT_C126870 subClassOf NCIT_C2991 @default.
- NCIT_C126870 subClassOf NCIT_C3235 @default.
- NCIT_C126870 subClassOf NCIT_C4873 @default.
- NCIT_C126870 subClassOf NCIT_C53529 @default.
- NCIT_C126870 subClassOf NCIT_C53543 @default.
- NCIT_C126870 subClassOf NCIT_C53547 @default.
- NCIT_C126870 subClassOf NCIT_C7057 @default.
- NCIT_C126870 subClassOf NCIT_C84615 @default.
- NCIT_C126870 subClassOf NCIT_C97089 @default.