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- NCIT_C126873 IAO_0000115 "A congenital disorder of glycosylation sub-type caused by mutation(s) in the ALG12 gene, dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase." @default.
- NCIT_C126873 NCIT_NHC0 "C126873" @default.
- NCIT_C126873 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C126873 NCIT_P108 "Congenital Disorder of Glycosylation Type Ig" @default.
- NCIT_C126873 NCIT_P207 "C2931001" @default.
- NCIT_C126873 NCIT_P322 "Cellosaurus" @default.
- NCIT_C126873 NCIT_R176 NCIT_C16612 @default.
- NCIT_C126873 NCIT_R176 NCIT_C191657 @default.
- NCIT_C126873 NCIT_R176 NCIT_C21281 @default.
- NCIT_C126873 NCIT_R176 NCIT_C25870 @default.
- NCIT_C126873 NCIT_R176 NCIT_C26147 @default.
- NCIT_C126873 normalizedInformationContent "100" @default.
- NCIT_C126873 referenceCount "1" @default.
- NCIT_C126873 hasExactSynonym "CDGIg" @default.
- NCIT_C126873 hasExactSynonym "Congenital Disorder of Glycosylation Type Ig" @default.
- NCIT_C126873 inSubset NCIT_C165258 @default.
- NCIT_C126873 inSubset NCIT_C192842 @default.
- NCIT_C126873 type Class @default.
- NCIT_C126873 isDefinedBy ncit.owl @default.
- NCIT_C126873 label "Congenital Disorder of Glycosylation Type Ig" @default.
- NCIT_C126873 subClassOf B1f865f1e4801fdf8c0272084b4042964 @default.
- NCIT_C126873 subClassOf Ba062b9c8ef76839c29ac0759b1761783 @default.
- NCIT_C126873 subClassOf NCIT_C126873 @default.
- NCIT_C126873 subClassOf NCIT_C28193 @default.
- NCIT_C126873 subClassOf NCIT_C2991 @default.
- NCIT_C126873 subClassOf NCIT_C3235 @default.
- NCIT_C126873 subClassOf NCIT_C4873 @default.
- NCIT_C126873 subClassOf NCIT_C53529 @default.
- NCIT_C126873 subClassOf NCIT_C53543 @default.
- NCIT_C126873 subClassOf NCIT_C53547 @default.
- NCIT_C126873 subClassOf NCIT_C7057 @default.
- NCIT_C126873 subClassOf NCIT_C84615 @default.
- NCIT_C126873 subClassOf NCIT_C97089 @default.