Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_assertion description "[LS patients with MSH2 mutations are at an increased risk for not only UTUC but also BCa and could be offered appropriate screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_assertion evidence source_evidence_literature NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_assertion SIO_000772 22883484 NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_assertion wasDerivedFrom befree-20140225 NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_assertion wasGeneratedBy ECO_0000203 NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP621789.RAj_RyJq-hVAMDjGWSqdzBZx0wbERszbh0cV1yM_-i-mA130_provenance.