Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_assertion wasGeneratedBy ECO_0000203 NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_assertion wasDerivedFrom befree-20140225 NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_assertion SIO_000772 21389716 NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_assertion evidence source_evidence_literature NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_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." NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP829842.RAVFuwn_73NPSh-EqKxA31U-iB_VzccO8H_B2q-G7wzHg130_provenance.