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- NCIT_C84569 IAO_0000115 "A genetic inherited disorder caused by mutations in the ASL gene. It is characterized by accumulation of ammonia in the blood. It presents with lethargy in the first few days of life, accompanied by developmental delay and mental retardation." @default.
- NCIT_C84569 NCIT_NHC0 "C84569" @default.
- NCIT_C84569 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84569 NCIT_P108 "Argininosuccinic Aciduria" @default.
- NCIT_C84569 NCIT_P207 "C0268547" @default.
- NCIT_C84569 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84569 NCIT_P322 "NICHD" @default.
- NCIT_C84569 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84569 NCIT_R176 NCIT_C192689 @default.
- NCIT_C84569 NCIT_R176 NCIT_C21281 @default.
- NCIT_C84569 NCIT_R176 NCIT_C21282 @default.
- NCIT_C84569 normalizedInformationContent "100" @default.
- NCIT_C84569 referenceCount "1" @default.
- NCIT_C84569 hasExactSynonym "Argininosuccinate Lyase Deficiency" @default.
- NCIT_C84569 hasExactSynonym "Argininosuccinic Aciduria" @default.
- NCIT_C84569 inSubset NCIT_C165258 @default.
- NCIT_C84569 inSubset NCIT_C192842 @default.
- NCIT_C84569 inSubset NCIT_C90259 @default.
- NCIT_C84569 inSubset NCIT_C99147 @default.
- NCIT_C84569 type Class @default.
- NCIT_C84569 isDefinedBy ncit.owl @default.
- NCIT_C84569 label "Argininosuccinic Aciduria" @default.
- NCIT_C84569 subClassOf B19c7c4f37e8b5d35de2ba7d202758b9c @default.
- NCIT_C84569 subClassOf B658967c961ba04d7c71d8af9e198e74b @default.
- NCIT_C84569 subClassOf NCIT_C2991 @default.
- NCIT_C84569 subClassOf NCIT_C4873 @default.
- NCIT_C84569 subClassOf NCIT_C53529 @default.
- NCIT_C84569 subClassOf NCIT_C53543 @default.
- NCIT_C84569 subClassOf NCIT_C53547 @default.
- NCIT_C84569 subClassOf NCIT_C7057 @default.
- NCIT_C84569 subClassOf NCIT_C84569 @default.