Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_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 ratio?=?0.58, 95% confidence interval: 0.33-1.05, p?=?0.07).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_assertion evidence source_evidence_literature NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_assertion SIO_000772 20731606 NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_assertion wasDerivedFrom befree-20150227 NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_assertion wasGeneratedBy ECO_0000203 NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP440373.RAW0gHgDFyRnJ75clGxRrYaxSZFFRIVYwtm7Q_1WFPdIk130_provenance.