Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_assertion description "[The present findings regarding genetic polymorphisms, determination of serum sPLA(2)-IIa, and prognosis in CVD patients are consistent with a genuine causal relationship and thus might point to a valid drug target for prevention of secondary CVD events.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_assertion evidence source_evidence_literature NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_assertion SIO_000772 21799821 NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_assertion wasDerivedFrom befree-20150227 NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_assertion wasGeneratedBy ECO_0000203 NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP627857.RAWexvhzPFdHvO49tRDXb1klBccuIstYDkAJNlhN3IsAE130_provenance.