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- NCIT_C84568 IAO_0000115 "A rare autosomal recessive metabolic disorder characterized by a deficiency of the enzyme arginase resulting in accumulation of arginine and urea in the blood and cerebrospinal fluid. Signs and symptoms include developmental delays, spasticity, ataxia, seizures and mental retardation." @default.
- NCIT_C84568 NCIT_NHC0 "C84568" @default.
- NCIT_C84568 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84568 NCIT_P108 "Argininemia" @default.
- NCIT_C84568 NCIT_P207 "C0268548" @default.
- NCIT_C84568 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84568 NCIT_R176 NCIT_C103927 @default.
- NCIT_C84568 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84568 NCIT_R176 NCIT_C21281 @default.
- NCIT_C84568 NCIT_R176 NCIT_C25804 @default.
- NCIT_C84568 normalizedInformationContent "100" @default.
- NCIT_C84568 referenceCount "1" @default.
- NCIT_C84568 hasExactSynonym "Argininemia" @default.
- NCIT_C84568 hasExactSynonym "Hyperargininemia" @default.
- NCIT_C84568 inSubset NCIT_C165258 @default.
- NCIT_C84568 inSubset NCIT_C192842 @default.
- NCIT_C84568 type Class @default.
- NCIT_C84568 isDefinedBy ncit.owl @default.
- NCIT_C84568 label "Argininemia" @default.
- NCIT_C84568 subClassOf B8b51cd8f87834c07d40fa18593a0c62b @default.
- NCIT_C84568 subClassOf Bfb54ef149a6a6d7a4d12070816bd2260 @default.
- NCIT_C84568 subClassOf NCIT_C2991 @default.
- NCIT_C84568 subClassOf NCIT_C3235 @default.
- NCIT_C84568 subClassOf NCIT_C34816 @default.
- NCIT_C84568 subClassOf NCIT_C4873 @default.
- NCIT_C84568 subClassOf NCIT_C53529 @default.
- NCIT_C84568 subClassOf NCIT_C53543 @default.
- NCIT_C84568 subClassOf NCIT_C53547 @default.
- NCIT_C84568 subClassOf NCIT_C7057 @default.
- NCIT_C84568 subClassOf NCIT_C84568 @default.
- NCIT_C84568 subClassOf NCIT_C97090 @default.