Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion description "[Our results confirm the significant contribution of ARX mutations in the etiology of MR, especially in this group of patients selected for XLMR (3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion evidence source_evidence_literature NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion SIO_000772 16523516 NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion wasDerivedFrom befree-20140225 NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_assertion wasGeneratedBy ECO_0000203 NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP308786.RAh5M6RimwdP4jA_74HTvpQ_UUOEI79U9DScw-n4ofvBM130_provenance.