Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_assertion description "[Polymorphism of apoprotein E (APOE), methylenetetrahydrofolate reductase (MTHFR) and paraoxonase (PON1) genes in patients with cerebrovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_assertion evidence source_evidence_literature NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_assertion SIO_000772 11388660 NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_assertion wasDerivedFrom gad-20150221 NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_assertion wasGeneratedBy ECO_0000203 NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP70303.RA29xv0gs7vd0OHyY9PcTrfNgj46Uo_5HG1ZD1g5LrJRE130_provenance.