Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_assertion description "[Association of deletion polymorphism in GSTT1 and GSTM1 genes and polymorphic variant A313G of GSTP1 gene with cirrhosis diseases and 4-year survival rate for the Tomsk region (West Siberia) patients were tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_assertion evidence source_evidence_literature NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_assertion SIO_000772 20608166 NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_assertion wasDerivedFrom gad-20130706 NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_assertion wasGeneratedBy ECO_0000203 NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- gad-20130706 importedOn "2013-07-06" NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.