Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_assertion description "[The SOD2 Val/Val genotype may increase the risk of NSCLC carried by XRCC1 and p53 polymorphisms, particularly for adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_assertion evidence source_evidence_literature NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_assertion SIO_000772 15534883 NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_assertion wasDerivedFrom befree-2016 NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_assertion wasGeneratedBy ECO_0000203 NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.
- befree-2016 importedOn "2016-02-19" NP468122.RA0ohQ5p7Zg2s2VUe2HaKWI1yp-635RD_3uGdqJV9HQIY130_provenance.