Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_assertion description "[Common genetic variants in four genes (GREM1, EYA1, ROBO2 and UPK3A) show a trend towards association with the development of primary VUR (GREM1, EYA1, ROBO2) or duplex collecting system (EYA1 and UPK3A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_assertion evidence source_evidence_literature NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_assertion SIO_000772 22558067 NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_assertion wasDerivedFrom befree-2016 NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_assertion wasGeneratedBy ECO_0000203 NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.
- befree-2016 importedOn "2016-02-19" NP979638.RAwNdtpkgwm2to9qWdpwjj0Vpagah9VrOF2SRfvyhSF4I130_provenance.