. . . . . . . "[Common variations rs6966 (3' UTR of PPP1R13L, chr 19q13.32, P?=?4.55?�?10(-9)) and rs414580 (intron 2 of MSR1, chr 8p22, P?=?6.09?�?10(-8)) were significantly associated with ALL.]. 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 . "2017-10-17T13:14:44+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .