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- NCIT_C190816 IAO_0000115 "Human CRADD wild-type allele is located in the vicinity of 12q22 and is approximately 217 kb in length. This allele, which encodes death domain-containing protein CRADD, is involved in the promotion of apoptosis. Mutation of the gene is associated with autosomal recessive intellectual developmental disorder 34 with variant lissencephaly." @default.
- NCIT_C190816 NCIT_NHC0 "C190816" @default.
- NCIT_C190816 NCIT_P100 "603454" @default.
- NCIT_C190816 NCIT_P102 "U84388" @default.
- NCIT_C190816 NCIT_P106 "Gene or Genome" @default.
- NCIT_C190816 NCIT_P108 "CRADD wt Allele" @default.
- NCIT_C190816 NCIT_P208 "CL1799294" @default.
- NCIT_C190816 NCIT_P321 "8738" @default.
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- NCIT_C190816 NCIT_R41 NCIT_C14225 @default.
- NCIT_C190816 NCIT_R41 NCIT_C14234 @default.
- NCIT_C190816 NCIT_R41 NCIT_C14250 @default.
- NCIT_C190816 NCIT_R41 NCIT_C14262 @default.
- NCIT_C190816 NCIT_R41 NCIT_C14282 @default.
- NCIT_C190816 NCIT_R41 NCIT_C25796 @default.
- NCIT_C190816 NCIT_R41 NCIT_C79740 @default.
- NCIT_C190816 normalizedInformationContent "100" @default.
- NCIT_C190816 referenceCount "1" @default.
- NCIT_C190816 hasExactSynonym "CASP2 and RIPK1 Domain Containing Adaptor with Death Domain wt Allele" @default.
- NCIT_C190816 hasExactSynonym "CRADD wt Allele" @default.
- NCIT_C190816 hasExactSynonym "MRT34" @default.
- NCIT_C190816 hasExactSynonym "RAIDD" @default.
- NCIT_C190816 hasExactSynonym "RIP-Associated ICH1/CED3-Homologous Protein With Death Domain Gene" @default.
- NCIT_C190816 type Class @default.
- NCIT_C190816 isDefinedBy ncit.owl @default.
- NCIT_C190816 label "CRADD wt Allele" @default.
- NCIT_C190816 subClassOf NCIT_C16612 @default.
- NCIT_C190816 subClassOf NCIT_C190815 @default.
- NCIT_C190816 subClassOf NCIT_C190816 @default.
- NCIT_C190816 subClassOf NCIT_C20348 @default.
- NCIT_C190816 subClassOf NCIT_C20462 @default.
- NCIT_C190816 equivalentClass B1a146ea708f6443c6bfdf677cadab643 @default.
- NCIT_C190816 equivalentClass B5c5df62b61660dc8002dab6892adbb9a @default.