Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_assertion description "[Although GSTT1 null genotype was insignificantly lower in ALL patients (20.9%) than controls (22.7%), it was significantly underrepresented in ANLL patients (6.5%) (P = 0.05, OR 0.24, 95% CI 0.05-1.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_assertion evidence source_evidence_literature NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_assertion SIO_000772 12827651 NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_assertion wasDerivedFrom befree-20150227 NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_assertion wasGeneratedBy ECO_0000203 NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP440355.RA1pbWFW18VuEe-pWFQ0NBcTlG_yOehEs5x3RqZDiMESE130_provenance.