Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_assertion description "[After the adjustment for covariates, the carriers of minor D allele of RGS2-rs34717272 had an increased hypertension risk (DD+ID vs. II; odds ratio=1.19; 95% confidence interval, 1.04-1.35; P value after the Bonferroni correction=0.009 x 5=0.045).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_assertion evidence source_evidence_literature NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_assertion SIO_000772 18496125 NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_assertion wasDerivedFrom gad-20150221 NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_assertion wasGeneratedBy ECO_0000203 NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123361.RAKMW1BUZ0HljdBD0oR8lLY12tDXITLn_E2O9P_jg4smQ130_provenance.