Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_assertion description "[The frequency of the -403G/A and -28C/G polymorphisms was evaluated in the entire sample, which consisted of 118 patients subjected to percutaneous coronary intervention (PCI) without ISR on angiographic re-evaluation (no IRS group), 74 CAD patients with ISR on angiographic re-evaluation (IRS group) and 146 controls without angiographic evidence of CAD (no CAD group).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_assertion evidence source_evidence_literature NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_assertion SIO_000772 19201454 NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_assertion wasDerivedFrom befree-20140225 NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_assertion wasGeneratedBy ECO_0000203 NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380433.RAH1byS3OSBgJiwpdLWNytYjTttv_vkOryiINd3Rfq6Ng130_provenance.