Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_assertion description "[The combination of the XPC-PAT and the XPA variant alleles significantly increased GC risk (OR=2.15; 95% CI 1.17-3.93, P=0.0092).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_assertion evidence source_evidence_literature NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_assertion SIO_000772 20817763 NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_assertion wasDerivedFrom befree-20150227 NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_assertion wasGeneratedBy ECO_0000203 NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779127.RAaYV2YLGBsuUjXrf8qETUs50b9Zbdg21kChTNq_StgWI130_provenance.