Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_assertion description "[The data obtained showed no statistically significant association of allelic or genotypic variants of CYP1A1*2B (OR = 1.06; 95% CI = 0.49-2.29) and GSTP1*B (OR = 1.40; 95% CI = 0.70-2.79) with OSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_assertion evidence source_evidence_literature NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_assertion SIO_000772 17160265 NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_assertion wasDerivedFrom befree-20140225 NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_assertion wasGeneratedBy ECO_0000203 NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP329231.RA6uyUajnzvUfSz0r2n7SyJqRsdRfnfpbQ7UcuLNBqtyI130_provenance.