. . . . . . . "[We used next generation sequencing of the whole gene (n�=�700), exon 2 Sanger sequencing (n�=�2634), p.R47H genotyping (n�=�3518), and genome wide association study imputation (n�=�13,048) to determine whether TREM2 variants are risk factors or phenotypic modifiers in patients with AD (n�=�1002), frontotemporal dementia (n�=�358), sporadic (n�=�2500), and variant (n�=�115) Creutzfeldt-Jakob disease (CJD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:18:34+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .