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- NCIT_C102441 IAO_0000115 "Human CHD8 wild-type allele is located in the vicinity of 14q11.2 and is approximately 71 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 8, is involved in both transcriptional regulation and chromatin modification." @default.
- NCIT_C102441 NCIT_NHC0 "C102441" @default.
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- NCIT_C102441 NCIT_P102 "AB046784" @default.
- NCIT_C102441 NCIT_P106 "Gene or Genome" @default.
- NCIT_C102441 NCIT_P108 "CHD8 wt Allele" @default.
- NCIT_C102441 NCIT_P207 "C3540049" @default.
- NCIT_C102441 NCIT_P321 "57680" @default.
- NCIT_C102441 NCIT_P98 "Mutation of the CHD8 gene may be associated with autism. (Nature. 2012; 485:237-241 and Nature. 2012; 485:246-250.)" @default.
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- NCIT_C102441 hasExactSynonym "Axis Duplication Inhibitor Gene" @default.
- NCIT_C102441 hasExactSynonym "CHD8 wt Allele" @default.
- NCIT_C102441 hasExactSynonym "Chromodomain Helicase DNA Binding Protein 8 wt Allele" @default.
- NCIT_C102441 hasExactSynonym "DKFZp686N17164" @default.
- NCIT_C102441 hasExactSynonym "DUPLIN" @default.
- NCIT_C102441 hasExactSynonym "HELSNF1" @default.
- NCIT_C102441 hasExactSynonym "KIAA1564" @default.
- NCIT_C102441 type Class @default.
- NCIT_C102441 isDefinedBy ncit.owl @default.
- NCIT_C102441 label "CHD8 wt Allele" @default.
- NCIT_C102441 subClassOf NCIT_C102440 @default.
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