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- NCIT_C93070 IAO_0000115 "Human CUL4B wild-type allele is located in the vicinity of Xq23 and is approximately 51 kb in length. This allele, which encodes cullin-4B protein, is involved in the mediation of protein ubiquitination. Mutation of the gene is associated with both mental retardation, X-linked, syndromic type 15 and Cabezas syndrome." @default.
- NCIT_C93070 NCIT_NHC0 "C93070" @default.
- NCIT_C93070 NCIT_P100 "300304" @default.
- NCIT_C93070 NCIT_P102 "U58091" @default.
- NCIT_C93070 NCIT_P106 "Gene or Genome" @default.
- NCIT_C93070 NCIT_P108 "CUL4B wt Allele" @default.
- NCIT_C93070 NCIT_P207 "C2985421" @default.
- NCIT_C93070 NCIT_P321 "8450" @default.
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- NCIT_C93070 NCIT_R37 NCIT_C61559 @default.
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- NCIT_C93070 NCIT_R41 NCIT_C14282 @default.
- NCIT_C93070 NCIT_R41 NCIT_C25796 @default.
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- NCIT_C93070 normalizedInformationContent "100" @default.
- NCIT_C93070 referenceCount "1" @default.
- NCIT_C93070 hasExactSynonym "CUL4B wt Allele" @default.
- NCIT_C93070 hasExactSynonym "Cullin 4B wt Allele" @default.
- NCIT_C93070 hasExactSynonym "DKFZp686F1470" @default.
- NCIT_C93070 hasExactSynonym "KIAA0695" @default.
- NCIT_C93070 hasExactSynonym "MRXHF2" @default.
- NCIT_C93070 hasExactSynonym "MRXSC" @default.
- NCIT_C93070 hasExactSynonym "SFM2" @default.
- NCIT_C93070 type Class @default.
- NCIT_C93070 isDefinedBy ncit.owl @default.
- NCIT_C93070 label "CUL4B wt Allele" @default.
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- NCIT_C93070 subClassOf NCIT_C16612 @default.
- NCIT_C93070 subClassOf NCIT_C20194 @default.
- NCIT_C93070 subClassOf NCIT_C26074 @default.
- NCIT_C93070 subClassOf NCIT_C93069 @default.
- NCIT_C93070 subClassOf NCIT_C93070 @default.