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- NCIT_C126558 IAO_0000115 "A rare disorder caused by mutation in the LMF1 gene resulting in combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders." @default.
- NCIT_C126558 NCIT_NHC0 "C126558" @default.
- NCIT_C126558 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C126558 NCIT_P108 "Combined Lipase Deficiency" @default.
- NCIT_C126558 NCIT_P207 "C1855498" @default.
- NCIT_C126558 NCIT_P322 "Cellosaurus" @default.
- NCIT_C126558 NCIT_R176 NCIT_C134605 @default.
- NCIT_C126558 NCIT_R176 NCIT_C16612 @default.
- NCIT_C126558 NCIT_R176 NCIT_C25802 @default.
- NCIT_C126558 normalizedInformationContent "100" @default.
- NCIT_C126558 referenceCount "1" @default.
- NCIT_C126558 hasExactSynonym "Combined Lipase Deficiency" @default.
- NCIT_C126558 inSubset NCIT_C165258 @default.
- NCIT_C126558 inSubset NCIT_C192842 @default.
- NCIT_C126558 type Class @default.
- NCIT_C126558 isDefinedBy ncit.owl @default.
- NCIT_C126558 label "Combined Lipase Deficiency" @default.
- NCIT_C126558 subClassOf B12fc697dab2f6ec86f07c03f4257c5de @default.
- NCIT_C126558 subClassOf Bc42549ce9e977abc1a816ff60b8337d9 @default.
- NCIT_C126558 subClassOf NCIT_C126558 @default.
- NCIT_C126558 subClassOf NCIT_C2991 @default.
- NCIT_C126558 subClassOf NCIT_C4873 @default.
- NCIT_C126558 subClassOf NCIT_C53529 @default.
- NCIT_C126558 subClassOf NCIT_C53543 @default.
- NCIT_C126558 subClassOf NCIT_C53547 @default.
- NCIT_C126558 subClassOf NCIT_C7057 @default.