Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_assertion description "[The most remarkable risk was seen for the small cell carcinoma among subjects with the GSTP1*B/*B genotype and concurrent lack of the GSTM1 gene (OR = 6.9, 95% CI 1.6-30.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_assertion evidence source_evidence_literature NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_assertion SIO_000772 12189190 NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_assertion wasDerivedFrom befree-20140225 NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_assertion wasGeneratedBy ECO_0000203 NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP757643.RAZ01edOmCdUoorFjNkSE5nNfjgm6l_O9oJIsZlSeFjVU130_provenance.