. . . . . . . . . . . . "[study failed to replicate an association of the common GABRB3 exon 1a promoter SNP rs4906902 with childhood absence epilepsy.no evidence that the common functional C-variant confers a substantial epileptogenic effect to a broad spectrum of IGE syndromes ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:33:14+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .