Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_assertion description "[Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_assertion evidence source_evidence_literature NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_assertion SIO_000772 20594303 NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_assertion wasDerivedFrom befree-20150227 NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_assertion wasGeneratedBy ECO_0000203 NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP229912.RAIK-EEv0URS0JWX6rPDO58vzLOE2ocI9jW-uEbPpOLbM130_provenance.