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- NCIT_C75310 IAO_0000115 "Human CHD7 wild-type allele is located in the vicinity of 8q12.2 and is approximately 188 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 7, may be involved in both transcriptional regulation and chromatin modification. Mutation of the gene is associated with CHARGE syndrome." @default.
- NCIT_C75310 NCIT_NHC0 "C75310" @default.
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- NCIT_C75310 NCIT_P102 "AB037837" @default.
- NCIT_C75310 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75310 NCIT_P107 "CHD7 wt Allele" @default.
- NCIT_C75310 NCIT_P108 "CHD7 wt Allele" @default.
- NCIT_C75310 NCIT_P207 "C2698725" @default.
- NCIT_C75310 NCIT_P321 "55636" @default.
- NCIT_C75310 NCIT_P322 "CTRP" @default.
- NCIT_C75310 NCIT_P366 "CHD7_wt_Allele" @default.
- NCIT_C75310 NCIT_P98 "Variants of the CHD7 gene are associated with idiopathic scoliosis type 3. (UniProt)" @default.
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- NCIT_C75310 hasExactSynonym "CHD7 wt Allele" @default.
- NCIT_C75310 hasExactSynonym "Chromodomain Helicase DNA Binding Protein 7 wt Allele" @default.
- NCIT_C75310 hasExactSynonym "FLJ20357" @default.
- NCIT_C75310 hasExactSynonym "FLJ20361" @default.
- NCIT_C75310 hasExactSynonym "IS3" @default.
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- NCIT_C75310 type Class @default.
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- NCIT_C75310 label "CHD7 wt Allele" @default.
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