Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_assertion description "[As to GSTP1 and PON1 192 polymorphisms, the mutant Val and R alleles, respectively, were associated with a decreased risk of developing BC, while polymorphisms in PON1 55 and GLO1 were associated with an increased risk of this neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_assertion evidence source_evidence_literature NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_assertion SIO_000772 19379515 NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_assertion wasDerivedFrom befree-20140225 NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_assertion wasGeneratedBy ECO_0000203 NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP913923.RAmPEwZ32pN5KoKNklSsIlqCdrX9YnTzglSP9bWQM-gK0130_provenance.