Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_assertion description "[However, the frequency of GSTT1 null genotype was higher among controls (28.7%) than AML cases (21.6%), which showed a protective effect of the null genotype (odds ratioa=a0.58, 95% confidence interval: 0.33-1.05, pa=a0.07).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_assertion evidence source_evidence_literature NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_assertion SIO_000772 20731606 NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_assertion wasDerivedFrom gad-20150221 NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_assertion wasGeneratedBy ECO_0000203 NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP50552.RAcJ5jUIcCfaG6gUvtLqPUpPSuC5_ZU93lCxHFcx64kTo130_provenance.