Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_assertion wasGeneratedBy ECO_0000203 NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_assertion wasDerivedFrom befree-20140225 NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_assertion SIO_000772 21389716 NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_assertion evidence source_evidence_literature NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_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." NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP804639.RAc5vDTvbMOsKg_3ehJRzimffsLaDwPQoUh5HVB50EWs8130_provenance.