Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_assertion description "[In comparison with genetically undefined patients, LRRK2 mutation carriers had more severe motor symptoms (median Unified Parkinson's Disease Rating Scale scores approximately 1.6 times higher, p<0.001), a higher rate of dyskinesia (OR 4.21, p=0.002) and use of dopamine agonists (OR 3.64, p<0.001), and less postural tremor (OR 0.21, p<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_assertion evidence source_evidence_literature NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_assertion SIO_000772 19726410 NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_assertion wasDerivedFrom befree-20140225 NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_assertion wasGeneratedBy ECO_0000203 NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP429705.RAonoHvYtHczQ6Mzp7JtIZnLqGLT1WcucUKwr8M2vm03o130_provenance.