. . . . . . . . . . . . "[genes causing hereditary hemorrhagic telangiectasia (HHT), i.e.endoglin (ENG) and activin receptor-like kinase 1 (ACVRL1), have a relatively high mutation rate.all the four ENG mutations and one of the ACVRL1 mutations were new]. 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 . "2015-08-25T14:39:43+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .