Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_assertion description "[None of the 4 remaining polymorphisms showed a significant association with AAA: IL-1RN (+2018) C>T (p = 0.061), IL-1B (+3954) C>T (p = 0.51), IL-1B (-511) C>T (p = 0.61) and IL-1A (+4845) G>T (p = 0.81).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_assertion evidence source_evidence_literature NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_assertion SIO_000772 16268484 NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_assertion wasDerivedFrom befree-2016 NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_assertion wasGeneratedBy ECO_0000203 NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.
- befree-2016 importedOn "2016-02-19" NP520981.RADF34Q98NQw1ZqGDEpKRPP1NM8jQBLl6drIXsRegmMLE130_provenance.