Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_assertion wasGeneratedBy ECO_0000203 NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_assertion wasDerivedFrom befree-20150227 NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_assertion SIO_000772 18573513 NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_assertion evidence source_evidence_literature NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.
- NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_assertion description "[The PCR study revealed that there is no significant difference in the allelic variants in GSTM1 between OSF and normal, while GSTT1 null gene showed significantly higher frequencies in this precancerous condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437896.RArs9UyLybW4SYjsv4AOWAqFA288V3wzQmOUz-q34H8Xo130_provenance.