Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_assertion description "[However, weak to absent GPx3 staining was observed in Barrett's dysplasia and adenocarcinoma samples where the promoter was hypermethylated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_assertion evidence source_evidence_literature NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_assertion SIO_000772 16229808 NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_assertion wasDerivedFrom befree-20140225 NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_assertion wasGeneratedBy ECO_0000203 NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP328637.RAJFtC5vsyoEHPXcG-ZaxkfcV0ED4mgL9WmSNzoJRiziM130_provenance.