. . . . . . . . . . . . "[Of the 10 candidate SNPs analyzed in this pilot study, the variant allele of the non-synonymous SNP, VCAM1 G1238C, may be associated with protection from stroke (OR 0.35, 95% CI 0.15-0.83, P=0.04). Further study is required to confirm the importance of this variant in VCAM1 as a clinically useful modifier of outcome in SS disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2013-07-06"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:32:27+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .