Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_assertion description "[In all 3 the AGTR1 1166C allele was significantly more common in AAA patients than controls (overall adjusted OR 1.60, 95% CI 1.32 to 1.93, P=1.1x10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_assertion evidence source_evidence_literature NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_assertion SIO_000772 18239157 NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_assertion wasDerivedFrom befree-2016 NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_assertion wasGeneratedBy ECO_0000203 NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.
- befree-2016 importedOn "2016-02-19" NP652881.RAMRzRPT53RV8cTfVXvRVN2NU0NRXrAudlWckprnjLaMc130_provenance.