Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion description "[Variation in the VEGF gene is weakly associated with IMT and the risk of AMI, but the effect can only be observed when the information of the SNPs is combined by constructing haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion evidence source_evidence_literature NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion SIO_000772 19089753 NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion wasDerivedFrom gad-20150221 NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion wasGeneratedBy ECO_0000203 NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance.