Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_assertion wasGeneratedBy ECO_0000203 NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_assertion wasDerivedFrom befree-20150227 NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_assertion SIO_000772 19005247 NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_assertion evidence source_evidence_literature NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.
- NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_assertion description "[Ninety-nine patients were tested for the presence of common polymorphisms related to thrombophilia (prothrombin and factor V Leiden) in order to assess genetic risk factors, and several parameters classically associated with vascular disorders (cardiovascular events, brain stroke and antiphospholipid syndrome) were evaluated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391537.RA3mHuZ3z0OI9CllheFPeIkgvP-ETpAtMdE1sy44UQX0A130_provenance.