. . . . . . . . . . . . "[study reports a new molecular defect in a family with true prothrombin deficiency; the mother was homozygous for a mutation Arg-Gln in position -39 of the propeptide controlled by exon 1; the son was heterozygosity for the same mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:39:40+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .