. . . . . . . "[In a Brazilian populaiton with beta Thalassemia, the beta 0 codon 39 nonsense mutation was the most frequent alteration (50.9%), followed by beta+ IVSI 110 G > A (18.1%), beta 0 IVSI 1 G > A (12.9%), beta+ IVSI 6 T > C (9.5%), and other rare mutations (8.6%]. 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 . "2017-10-17T13:13:13+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .