Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_assertion description "[In both the white and the black groups, there were no significant associations between these variants and essential hypertension (P > 0.05) or with serum electrolytes, creatinine or plasma renin activity (PRA) (ANOVA P > 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_assertion evidence source_evidence_literature NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_assertion SIO_000772 15201541 NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_assertion wasDerivedFrom befree-20150227 NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_assertion wasGeneratedBy ECO_0000203 NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP596932.RA5-sMmQbiXD2TwNoZnoIcdc4uiXa2TtEl0vuzRacXUf4130_provenance.