Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_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." NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_assertion evidence source_evidence_literature NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_assertion SIO_000772 16102903 NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_assertion wasDerivedFrom gad-20150221 NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_assertion wasGeneratedBy ECO_0000203 NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69454.RAbwmtUs85fab3l6aWlLuQ0KWvWh-tz56SHwu7--sPYr8130_provenance.