Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_assertion description "[We screened for the most common LRRK 2 mutation in a series of patients with Parkinson's Disease, Alzheimer's disease, Progressive Supranuclear Palsy, Multiple System Atrophy and frontotemporal dementia, as well as in neurologically normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_assertion evidence source_evidence_literature NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_assertion SIO_000772 16102903 NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_assertion wasDerivedFrom befree-2016 NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_assertion wasGeneratedBy ECO_0000203 NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.
- befree-2016 importedOn "2016-02-19" NP508948.RAfxqwp8YaMl4MvjwqtmW5s9Eozyqs1cukeSW6YPr8b9s130_provenance.