. . . . . . . . . . . . "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:45:31+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .