Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_assertion> ?p ?o ?g. }
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- NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_assertion type Assertion NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_head.
- NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_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." NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_provenance.
- NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_assertion evidence source_evidence_literature NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_provenance.
- NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_assertion SIO_000772 19726410 NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_provenance.
- NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_assertion wasDerivedFrom befree-20150227 NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_provenance.
- NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_assertion wasGeneratedBy ECO_0000203 NP967279.RANxu8YHfs_ggHdjdwS-sVb-Jsf4P3T_ilxBvAApyNZ98130_provenance.