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- source_evidence_literature type ECO_0000212 NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_assertion description "[Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_assertion evidence source_evidence_literature NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_assertion SIO_000772 23872634 NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_assertion wasDerivedFrom befree-20150227 NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_assertion wasGeneratedBy ECO_0000203 NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873873.RA1q4-S9p5laQZgel5q1Yi1MQM988xeTwOPGN1KKkNv2s130_provenance.