Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_assertion wasGeneratedBy ECO_0000203 NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_assertion wasDerivedFrom befree-20140225 NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_assertion SIO_000772 21389716 NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_assertion evidence source_evidence_literature NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_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." NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP214231.RA-kNCch-hb8Nnld80c460hpZCK9KeIs6ZwFmuBot2a_g130_provenance.