Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_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." NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_assertion evidence source_evidence_literature NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_assertion SIO_000772 17369504 NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_assertion wasDerivedFrom befree-20140225 NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_assertion wasGeneratedBy ECO_0000203 NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP508981.RAnmjq1mCJ56jGNEnVM_HafWJVVfSQXrAKsH1qPboir6o130_provenance.