Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_assertion description "[In the EVA study, the rs2781666 polymorphism was also associated with an increase in CCA-IMT (p = 0.010), a surrogate marker of MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_assertion evidence source_evidence_literature NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_assertion SIO_000772 17369504 NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_assertion wasDerivedFrom befree-20140225 NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_assertion wasGeneratedBy ECO_0000203 NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP862454.RApwgwVtRDrbQXubhfq9M0NX8Z7JnTplOP6oP0bwVhQQI130_provenance.