Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_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." NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_assertion evidence source_evidence_literature NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_assertion SIO_000772 12189190 NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_assertion wasDerivedFrom befree-20150227 NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_assertion wasGeneratedBy ECO_0000203 NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP439605.RA0FM3zbJNoheuZ754i5mNFHl1R64z6dr2stl8kr9zxSQ130_provenance.