Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_assertion wasGeneratedBy ECO_0000203 NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_assertion wasDerivedFrom befree-20150227 NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_assertion SIO_000772 21389716 NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_assertion evidence source_evidence_literature NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.
- NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_assertion description "[When GST polymorphism was analyzed in patients with AMI, GSTM1 null genotype frequencies were 0.24 and 0.21 among cases with coronary artery disease and controls, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_provenance.