Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_assertion> ?p ?o ?g. }
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- NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_assertion type Assertion NP438588.RA0AJWUDwFIzFNl-d2IscsBCC04oTe7SxTZ8dh6TDn60I130_head.
- 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.