Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_assertion description "[We investigated differences in the frequency of the polymorphism in the GPIIb subunit of the receptor HPA-3 (a and b allele) between patients with more extensive coronary thrombosis such as patients with ST segment elevation (STEMI) and those with less extensive coronary thrombosis such as those with non-ST elevation myocardial infarction (NSTEMI), unstable angina (UA) or chronic CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_assertion evidence source_evidence_literature NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_assertion SIO_000772 17561290 NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_assertion wasDerivedFrom befree-2016 NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_assertion wasGeneratedBy ECO_0000203 NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.
- befree-2016 importedOn "2016-02-19" NP614554.RAzepdlqFfylQ9rQvtFuAJslVmMfjbJ3BSGLhgtNiSE8g130_provenance.