. . . . . . . "[Presented is a pedigree with infancy-onset benign hereditary chorea (BHC) caused by a novel nonsense mutation in exon 3 (523G-- > T, E175X) of the TITF-1 (Nkx2.1) gene.]. 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 . "2017-10-17T13:16:43+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .