Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_assertion description "[Moreover, the frequency of endothelin-1 Lys198Asn polymorphism was investigated with respect to the prevalence of several actual or historical endorgan damages (renal disorder, coronary artery disease, vascular events, vascular damage, and congestive heart failure) in hypertensive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_assertion evidence source_evidence_literature NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_assertion SIO_000772 18923236 NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_assertion wasDerivedFrom befree-20140225 NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_assertion wasGeneratedBy ECO_0000203 NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681769.RABTeZbd44BBYg58PGFcgSODaJt8bh9R7WelPvlRETCok130_provenance.