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- NCIT_C132224 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the MRE11A gene, encoding double-strand break repair protein MRE11. It is characterized by progressive cerebellar degeneration resulting in ataxia and oculomotor apraxia." @default.
- NCIT_C132224 NCIT_NHC0 "C132224" @default.
- NCIT_C132224 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C132224 NCIT_P108 "Ataxia-Telangiectasia-Like Disorder 1" @default.
- NCIT_C132224 NCIT_P208 "CL520360" @default.
- NCIT_C132224 NCIT_P322 "Cellosaurus" @default.
- NCIT_C132224 NCIT_R176 NCIT_C153246 @default.
- NCIT_C132224 NCIT_R176 NCIT_C16612 @default.
- NCIT_C132224 NCIT_R176 NCIT_C19676 @default.
- NCIT_C132224 NCIT_R176 NCIT_C98167 @default.
- NCIT_C132224 normalizedInformationContent "100" @default.
- NCIT_C132224 referenceCount "1" @default.
- NCIT_C132224 hasExactSynonym "ATLD" @default.
- NCIT_C132224 hasExactSynonym "ATLD1" @default.
- NCIT_C132224 hasExactSynonym "Ataxia-Telangiectasia-Like Disorder 1" @default.
- NCIT_C132224 hasExactSynonym "Ataxia-Telangiectasia-Like Disorder" @default.
- NCIT_C132224 inSubset NCIT_C165258 @default.
- NCIT_C132224 inSubset NCIT_C192842 @default.
- NCIT_C132224 type Class @default.
- NCIT_C132224 isDefinedBy ncit.owl @default.
- NCIT_C132224 label "Ataxia-Telangiectasia-Like Disorder 1" @default.
- NCIT_C132224 subClassOf B6277e3f29cacece5de9c491b8cb41aa3 @default.
- NCIT_C132224 subClassOf Bf64a6df31adfecbb7286154047dd0017 @default.
- NCIT_C132224 subClassOf NCIT_C132224 @default.
- NCIT_C132224 subClassOf NCIT_C2991 @default.
- NCIT_C132224 subClassOf NCIT_C4873 @default.
- NCIT_C132224 subClassOf NCIT_C53529 @default.
- NCIT_C132224 subClassOf NCIT_C53543 @default.
- NCIT_C132224 subClassOf NCIT_C53547 @default.
- NCIT_C132224 subClassOf NCIT_C7057 @default.