Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_assertion description "[In this study we examined whether polymorphisms in GST genes influence the risk of CAD in a case-control group of South Asians, following our recent observation of such an association in Caucasians from the same region of the UK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_assertion evidence source_evidence_literature NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_assertion SIO_000772 12519635 NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_assertion wasDerivedFrom befree-20140225 NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_assertion wasGeneratedBy ECO_0000203 NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP309289.RA9BD-81iF0HHvpjQVn-4js68JN5MEMIp1KfWU6dpaW9M130_provenance.