Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_assertion description "[Our results further support that LRRK2 variants are an independent genetic risk factor for typical PD, but BDNF variants can greatly increase LRRK2-induced risk for patients with an onset age of older than 60 indicating an additive effect between the 2 genes, which might aid in studying the mechanism underlying LRRK2 parkinsonism and developing potential therapeutic strategies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_assertion evidence source_evidence_literature NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_assertion SIO_000772 21924942 NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_assertion wasDerivedFrom befree-2016 NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_assertion wasGeneratedBy ECO_0000203 NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.
- befree-2016 importedOn "2016-02-19" NP924385.RAiNPzModGBzQf5u5gMx63jWh2ULbDvAmXEtdNXkZjIwA130_provenance.