Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_assertion description "[The ND1 subunit gene of the mitochondrial NADH-ubiquinone oxidoreductase (complex I) is a hot spot for mutations causing Leber hereditary optic neuropathy and several mutations causing the mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome (MELAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_assertion evidence source_evidence_literature NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_assertion SIO_000772 16849371 NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_assertion wasDerivedFrom befree-20140225 NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_assertion wasGeneratedBy ECO_0000203 NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP582214.RA3QERY1hBASoLtMAf2loGfrtKO41EcdjlJgmGqpHl27Q130_provenance.