. . . . . . . "[Disease locus of 16q-autosomal dominant cerebellar ataxia was definitely confined to a 900-kb genomic region between the SNP04 and the -16C > T substitution in the puratrophin-1 gene in 16q22.1.]. 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 . "2017-10-17T13:18:18+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .