Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_assertion> ?p ?o ?g. }
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- NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_assertion type Assertion NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_head.
- NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_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." NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_provenance.
- NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_assertion evidence source_evidence_literature NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_provenance.
- NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_assertion SIO_000772 19726410 NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_provenance.
- NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_assertion wasDerivedFrom befree-20150227 NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_provenance.
- NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_assertion wasGeneratedBy ECO_0000203 NP967370.RAeea_whc6S3HXnE-raxNCXKp-p86egispYZY3b3LTuN8130_provenance.