. . . . . . . . . . . . "[The presence of an SCN1A mutation supports the diagnosis of Severe Myoclonic Epilepsy of Infancy (SMEI).]. 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 . "2016-05-13T12:43:37+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .