Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_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." NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_assertion evidence source_evidence_literature NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_assertion SIO_000772 16268484 NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_assertion wasDerivedFrom befree-20150227 NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_assertion wasGeneratedBy ECO_0000203 NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP490925.RAAG2XlZTO6FUJ5s7I1m4y1Q7AvSw0noFeov9TnmppfUM130_provenance.