. . . . . . . "[DNA sequencing identified a CTT (Leu) to TTT (Phe) mutation at codon 91 corresponding to the Hb Grey Lynn (Vientiane) [?91(FG3)Leu>Phe (?1) on ?1-globin gene and a C deletion between codons 36 and 37 on ?2-globin gene causing ?(+)-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:13:12+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .