Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_assertion description "[epsilon4 allele-containing (epsilon4+) genotypes were significantly associated with IS (odds ratio [OR], 1.11; 95% CI, 1.01 to 1.22) and SAH (OR, 1.42; 95% CI, 1.01 to 1.99) and nonsignificantly with ICH (OR, 1.16; 95% CI, 0.93 to 1.44), whereas epsilon2+ genotypes were associated with ICH (OR, 1.32; 95% CI, 1.01 to 1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_assertion evidence source_evidence_literature NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_assertion SIO_000772 16385096 NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_assertion wasDerivedFrom befree-20140225 NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_assertion wasGeneratedBy ECO_0000203 NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP406520.RA0WXDKePDxIE0ODbcMwpJ5r9aCFMaoETtTe7cEH5-1fI130_provenance.