A SNPshot of PubMed to associate genetic variants with drugs, diseases, and adverse reactions

► SNPshot is an automatically populated repository on genetic variants, relations to drugs, and associations with disease. ► Our methods yield a precision of 90-92% for the major entity types, and 76-84% for relations. ► SNPshot data covers PharmGKB and other repositories to more than 90based on 180,000 PubMed abstracts. ► SNPShot is publicly available for search and download at http://bioai4core.fulton.asu.edu/snpshot.