. . . . . . . "[Several of these variants are in or near genes with a biological rationale for conferring EOC risk, including ZFP36L1 and RAD51B for mucinous EOC (rs17106154, OR�=�1.17, P�=�0.029, n�=�1,483 cases), GRB10 for endometrioid and clear cell EOC (rs2190503, P�=�0.014, n�=�2,903 cases), and C22orf26/BPIL2 for LMP serous EOC (rs9609538, OR�=�0.86, P�=�0.0043, n�=�892 cases).]. 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 . "2017-10-17T13:15:52+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .