Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_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." NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_assertion evidence source_evidence_literature NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_assertion SIO_000772 16102903 NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_assertion wasDerivedFrom gad-20150221 NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_assertion wasGeneratedBy ECO_0000203 NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP94926.RA_JG5cu2toxy-ZANLAQD6g_PIyIZmKKXGo87F7mb8TDc130_provenance.