Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_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." NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_assertion evidence source_evidence_literature NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_assertion SIO_000772 12827651 NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_assertion wasDerivedFrom befree-2016 NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_assertion wasGeneratedBy ECO_0000203 NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.
- befree-2016 importedOn "2016-02-19" NP399655.RAAqG51TOphaHEh4147lqKsiRgU5ufJAXcEcS1mnaLhsY130_provenance.