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- NCIT_C114766 IAO_0000115 "A rare, autosomal recessive inherited disorder of long-chain fatty-acid oxidation caused by mutations in the CPT2 gene. The disease includes three main types: a lethal neonatal form, a severe infantile hepatocardiomuscular form, and a myopathic form." @default.
- NCIT_C114766 NCIT_NHC0 "C114766" @default.
- NCIT_C114766 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C114766 NCIT_P108 "Carnitine Palmitoyltransferase II Deficiency" @default.
- NCIT_C114766 NCIT_P207 "C1850734" @default.
- NCIT_C114766 NCIT_P322 "Cellosaurus" @default.
- NCIT_C114766 NCIT_R176 NCIT_C16612 @default.
- NCIT_C114766 NCIT_R176 NCIT_C200270 @default.
- NCIT_C114766 NCIT_R176 NCIT_C21281 @default.
- NCIT_C114766 NCIT_R176 NCIT_C25870 @default.
- NCIT_C114766 normalizedInformationContent "100" @default.
- NCIT_C114766 referenceCount "1" @default.
- NCIT_C114766 hasExactSynonym "CPT II Deficiency" @default.
- NCIT_C114766 hasExactSynonym "Carnitine Palmitoyltransferase II Deficiency" @default.
- NCIT_C114766 inSubset NCIT_C165258 @default.
- NCIT_C114766 inSubset NCIT_C192842 @default.
- NCIT_C114766 type Class @default.
- NCIT_C114766 isDefinedBy ncit.owl @default.
- NCIT_C114766 label "Carnitine Palmitoyltransferase II Deficiency" @default.
- NCIT_C114766 subClassOf B3b46e2a8f13b5bf4307c2aa6d01482c1 @default.
- NCIT_C114766 subClassOf B99b23ed2e164f2b27d983187cf37a93d @default.
- NCIT_C114766 subClassOf NCIT_C114766 @default.
- NCIT_C114766 subClassOf NCIT_C117115 @default.
- NCIT_C114766 subClassOf NCIT_C2991 @default.
- NCIT_C114766 subClassOf NCIT_C3235 @default.
- NCIT_C114766 subClassOf NCIT_C34816 @default.
- NCIT_C114766 subClassOf NCIT_C4873 @default.
- NCIT_C114766 subClassOf NCIT_C53529 @default.
- NCIT_C114766 subClassOf NCIT_C53543 @default.
- NCIT_C114766 subClassOf NCIT_C53547 @default.
- NCIT_C114766 subClassOf NCIT_C7057 @default.
- NCIT_C114766 subClassOf NCIT_C97092 @default.