Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_assertion description "[Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_assertion evidence source_evidence_literature NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_assertion SIO_000772 11872951 NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_assertion wasDerivedFrom befree-20140225 NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_assertion wasGeneratedBy ECO_0000203 NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP406334.RATO6CfLu3avjAqf_d52HM81qQgFbzaqn1oweXJVtK7hg130_provenance.