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- NCIT_C104141 IAO_0000115 "Human CRBN wild-type allele is located in the vicinity of 3p26.3 and is approximately 31 kb in length. This allele, which encodes protein cereblon protein, is involved in ubiquitin-mediated protein degradation. Mutations are associated with autosomal recessive nonsyndromic mental retardation." @default.
- NCIT_C104141 NCIT_NHC0 "C104141" @default.
- NCIT_C104141 NCIT_P100 "609262" @default.
- NCIT_C104141 NCIT_P102 "NM_016302" @default.
- NCIT_C104141 NCIT_P106 "Gene or Genome" @default.
- NCIT_C104141 NCIT_P107 "CRBN wt Allele" @default.
- NCIT_C104141 NCIT_P108 "CRBN wt Allele" @default.
- NCIT_C104141 NCIT_P207 "C3539702" @default.
- NCIT_C104141 NCIT_P321 "51185" @default.
- NCIT_C104141 NCIT_P322 "CTRP" @default.
- NCIT_C104141 normalizedInformationContent "100" @default.
- NCIT_C104141 referenceCount "1" @default.
- NCIT_C104141 hasExactSynonym "CRBN wt Allele" @default.
- NCIT_C104141 hasExactSynonym "Cereblon wt Allele" @default.
- NCIT_C104141 hasExactSynonym "MRT2A" @default.
- NCIT_C104141 hasExactSynonym "Mental Retardation, Non-Syndromic, Autosomal Recessive, 2A" @default.
- NCIT_C104141 inSubset NCIT_C116977 @default.
- NCIT_C104141 inSubset NCIT_C142799 @default.
- NCIT_C104141 inSubset NCIT_C142800 @default.
- NCIT_C104141 type Class @default.
- NCIT_C104141 isDefinedBy ncit.owl @default.
- NCIT_C104141 label "CRBN wt Allele" @default.
- NCIT_C104141 subClassOf NCIT_C104140 @default.
- NCIT_C104141 subClassOf NCIT_C104141 @default.
- NCIT_C104141 subClassOf NCIT_C16612 @default.
- NCIT_C104141 subClassOf NCIT_C26016 @default.