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- NCIT_C84771 IAO_0000115 "A genetic disorder of lipoprotein metabolism caused by mutations in the LPL and apolipoprotein (apo) C-II genes. It is characterized by increased levels of chylomicrons and triglycerides in the blood." @default.
- NCIT_C84771 NCIT_A13 NCIT_C104614 @default.
- NCIT_C84771 NCIT_A13 NCIT_C190082 @default.
- NCIT_C84771 NCIT_NHC0 "C84771" @default.
- NCIT_C84771 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84771 NCIT_P108 "Hyperlipoproteinemia, Type I" @default.
- NCIT_C84771 NCIT_P207 "C0023817" @default.
- NCIT_C84771 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84771 normalizedInformationContent "100" @default.
- NCIT_C84771 referenceCount "1" @default.
- NCIT_C84771 hasExactSynonym "Familial Essential Hyperlipemia" @default.
- NCIT_C84771 hasExactSynonym "Familial Hyperchylomicronemia" @default.
- NCIT_C84771 hasExactSynonym "Hyperlipoproteinemia Type 1A" @default.
- NCIT_C84771 hasExactSynonym "Hyperlipoproteinemia, Type I" @default.
- NCIT_C84771 hasExactSynonym "Lipoprotein Lipase Deficiency" @default.
- NCIT_C84771 inSubset NCIT_C165258 @default.
- NCIT_C84771 inSubset NCIT_C192842 @default.
- NCIT_C84771 type Class @default.
- NCIT_C84771 isDefinedBy ncit.owl @default.
- NCIT_C84771 label "Hyperlipoproteinemia, Type I" @default.
- NCIT_C84771 subClassOf NCIT_C2991 @default.
- NCIT_C84771 subClassOf NCIT_C3235 @default.
- NCIT_C84771 subClassOf NCIT_C34709 @default.
- NCIT_C84771 subClassOf NCIT_C4873 @default.
- NCIT_C84771 subClassOf NCIT_C53529 @default.
- NCIT_C84771 subClassOf NCIT_C53543 @default.
- NCIT_C84771 subClassOf NCIT_C53547 @default.
- NCIT_C84771 subClassOf NCIT_C7057 @default.
- NCIT_C84771 subClassOf NCIT_C84771 @default.