Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_assertion description "[We investigated the effect of the C181-->T polymorphism in exon 2 of the B2R gene in patients with end-stage renal disease (ESRD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_assertion evidence source_evidence_literature NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_assertion SIO_000772 15771553 NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_assertion wasDerivedFrom befree-20140225 NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_assertion wasGeneratedBy ECO_0000203 NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP331069.RAhiQ5CvNeYVFn2KOl0Au0r5VR_pEV_NLNOTCZGT60sn0130_provenance.