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- NCIT_C75490 IAO_0000115 "Human FOXP2 wild-type allele is located in the vicinity of 7q31 and is approximately 279 kb in length. This allele, which encodes forkhead box protein P2, plays a role in transcription during brain development. Mutations in the gene are associated with speech-language disorder 1 and a translocation t(5;7)(q22;q31.2) is associated with severe speech and language impairment." @default.
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- NCIT_C75490 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75490 NCIT_P108 "FOXP2 wt Allele" @default.
- NCIT_C75490 NCIT_P207 "C2700051" @default.
- NCIT_C75490 NCIT_P321 "93986" @default.
- NCIT_C75490 NCIT_P366 "FOXP2_wt_Allele" @default.
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- NCIT_C75490 hasExactSynonym "CAGH44" @default.
- NCIT_C75490 hasExactSynonym "DKFZp686H1726" @default.
- NCIT_C75490 hasExactSynonym "FOXP2 wt Allele" @default.
- NCIT_C75490 hasExactSynonym "Forkhead Box P2 wt Allele" @default.
- NCIT_C75490 hasExactSynonym "SPCH1" @default.
- NCIT_C75490 hasExactSynonym "TNRC10" @default.
- NCIT_C75490 type Class @default.
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- NCIT_C75490 label "FOXP2 wt Allele" @default.
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