Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_assertion description "[With all women included in the analysis, the Hp1-1 phenotype was associated with increased risk of CIN (OR contrasting Hp1-1 vs. Hp2-2 = 1.0; 95% CI: 0.6-1.5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_assertion evidence source_evidence_literature NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_assertion SIO_000772 17706188 NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_assertion wasDerivedFrom befree-20140225 NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_assertion wasGeneratedBy ECO_0000203 NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP705058.RAqrBnYYO-2HDrXg8q-uSam-nrNDOGjxhLYtNqsGUTBkQ130_provenance.