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- NCIT_C147993 IAO_0000115 "Human FGF12 wild-type allele is located within 3q28-q29 and is approximately 329 kb in length. This allele, which encodes fibroblast growth factor 12 protein, is involved in the development and function of the nervous system. Mutation of the gene is associated with early infantile epileptic encephalopathy." @default.
- NCIT_C147993 NCIT_NHC0 "C147993" @default.
- NCIT_C147993 NCIT_P100 "601513" @default.
- NCIT_C147993 NCIT_P102 "U66197" @default.
- NCIT_C147993 NCIT_P106 "Gene or Genome" @default.
- NCIT_C147993 NCIT_P108 "FGF12 wt Allele" @default.
- NCIT_C147993 NCIT_P208 "CL545848" @default.
- NCIT_C147993 NCIT_P321 "2257" @default.
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- NCIT_C147993 hasExactSynonym "EIEE47" @default.
- NCIT_C147993 hasExactSynonym "FGF-12" @default.
- NCIT_C147993 hasExactSynonym "FGF12 wt Allele" @default.
- NCIT_C147993 hasExactSynonym "FGF12B" @default.
- NCIT_C147993 hasExactSynonym "FHF-1" @default.
- NCIT_C147993 hasExactSynonym "FHF1" @default.
- NCIT_C147993 hasExactSynonym "Fibroblast Growth Factor 12 wt Allele" @default.
- NCIT_C147993 hasExactSynonym "Fibroblast Growth Factor 12B Gene" @default.
- NCIT_C147993 hasExactSynonym "Fibroblast Growth Factor FGF-12b Gene" @default.
- NCIT_C147993 type Class @default.
- NCIT_C147993 isDefinedBy ncit.owl @default.
- NCIT_C147993 label "FGF12 wt Allele" @default.
- NCIT_C147993 subClassOf NCIT_C147991 @default.
- NCIT_C147993 subClassOf NCIT_C147993 @default.
- NCIT_C147993 subClassOf NCIT_C16612 @default.
- NCIT_C147993 subClassOf NCIT_C18568 @default.
- NCIT_C147993 subClassOf NCIT_C21344 @default.