Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_assertion description "[Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_assertion evidence source_evidence_literature NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_assertion SIO_000772 21247928 NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_assertion wasDerivedFrom befree-2016 NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_assertion wasGeneratedBy ECO_0000203 NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.
- befree-2016 importedOn "2016-02-19" NP866342.RA3zGolhKbsHkUQRyHlFf3iEu7Flrzje5lOs3zAOGWN1o130_provenance.