Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_assertion description "[Besides identifying 8 SCN5A mutations in the present cohort, a KCNE3 T4A mutation was found in a 55-year-old male patient who had experienced several episodes of syncope.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_assertion evidence source_evidence_literature NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_assertion SIO_000772 22987075 NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_assertion wasDerivedFrom befree-20140225 NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_assertion wasGeneratedBy ECO_0000203 NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP355576.RAiZKKMiWoF23HaXKQfebWTB68uF8oGhRzA6tqOZOWJjQ130_provenance.