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- NCIT_C118514 IAO_0000115 "Human FGF13 wild-type allele is located in the vicinity of Xq26.3 and is approximately 591 kb in length. This allele, which encodes fibroblast growth factor 13 protein, is involved in microtubule polymerization, neural development and neuronal migration. Deletion of the region of the X chromosome where the gene is located is associated with Borjeson-Forssman-Lehmann syndrome." @default.
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- NCIT_C118514 NCIT_P106 "Gene or Genome" @default.
- NCIT_C118514 NCIT_P107 "FGF13 wt Allele" @default.
- NCIT_C118514 NCIT_P108 "FGF13 wt Allele" @default.
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- NCIT_C118514 referenceCount "1" @default.
- NCIT_C118514 hasExactSynonym "FGF-13" @default.
- NCIT_C118514 hasExactSynonym "FGF13 wt Allele" @default.
- NCIT_C118514 hasExactSynonym "FGF2" @default.
- NCIT_C118514 hasExactSynonym "FHF-2" @default.
- NCIT_C118514 hasExactSynonym "FHF2" @default.
- NCIT_C118514 hasExactSynonym "Fibroblast Growth Factor 13 wt Allele" @default.
- NCIT_C118514 hasExactSynonym "Fibroblast Growth Factor Homologous Factor 2 Gene" @default.
- NCIT_C118514 hasExactSynonym "RP6-27P15.3" @default.
- NCIT_C118514 inSubset NCIT_C116977 @default.
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- NCIT_C118514 label "FGF13 wt Allele" @default.
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