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- source_evidence_literature type ECO_0000212 NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_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." NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_assertion evidence source_evidence_literature NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_assertion SIO_000772 19726410 NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_assertion wasDerivedFrom befree-2016 NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_assertion wasGeneratedBy ECO_0000203 NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.
- befree-2016 importedOn "2016-02-19" NP760895.RAAVey46x7Hn7VNoPsK-D6PUnChH4hZQrBTOVyM9e_BIo130_provenance.