Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_assertion description "[Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_assertion evidence source_evidence_literature NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_assertion SIO_000772 11463728 NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_assertion wasDerivedFrom befree-20140225 NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_assertion wasGeneratedBy ECO_0000203 NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP579224.RAqcP5yVL6wn3qnpIb7cLoBGB_CvUnVH2Epnd8xL68lu8130_provenance.