. . . . . . . "[In our center, more than 30% (278/911) of kidney transplant (KTx) recipients were diagnosed with a causal nephropathy: Prevalence of rare genetic disorders in this group was 4.32% (12/278), including 2,8-dihydroxyadeninuria (2,8-DHA) disease (n�=�2), HNF-1B-associated nephropathy (n�=�2), UMOD-related nephropathy (n�=�5), Fabry disease (n�=�1), INF2 focal segmental glomerulosclerosis (n�=�1), and Senior-L�ken syndrome (n�=�1).]. 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 . "2017-10-17T13:17:09+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .