. . . . . . . . . . . . "[A novel mitochondrial DNA (mtDNA) transition (3733G-- > A) inducing the E143 K amino acid change at a very conserved site of the ND1 was identified in a family with six maternally related individuals with Leber's hereditary optic neuropathy (LHON) ]. 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 . "2014-10-02T12:33:17+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .