. . . . . . . . . . . . "[The variant CBS c.844_855ins68 -- that is, the allele carrying the insertion ('ins' or 'i') as opposed to the wild-type allele designated as deletion ('del' or 'd') -- was significantly overrepresented in meningioma patients (dd/ id/ii: 0.81/0.18/0.01) in comparison with the controls (dd/id/ii: 0.88/0.12/0; 2 df, chi-square 8.97, p = 0.011; multiple nominal regression with age and sex as covariables).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:48:12+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .