Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_assertion wasGeneratedBy ECO_0000203 NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_assertion wasDerivedFrom befree-20150227 NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_assertion SIO_000772 17510305 NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_assertion evidence source_evidence_literature NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.
- NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_assertion description "[The unadjusted odds ratio (OR) for sP-selectin >55.1 microg/L, representing the 95th percentile for controls, was 8.5 (95% CI, 3.7-23.3; P <0.001) and increased after adjustment for factor V Leiden, the prothrombin G20210A variant, increased factor VIII, and hyperhomocysteinemia (OR, 10.6; 95% CI, 4.1-31.2; P <0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391762.RAe62okDtFtgLuntFPNghwhg4JJ0muFY0dcAYD7Ka6yXM130_provenance.