Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_assertion description "[Pathogenic Lrrk2 Y1699C substitution observed in a large German-Canadian kindred presents a neurodegenerative disorder that is reminiscent of amyotrophic lateral sclerosis and Parkinsonism-Dementia Complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_assertion evidence source_evidence_literature NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_assertion SIO_000772 16865326 NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_assertion wasDerivedFrom befree-2016 NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_assertion wasGeneratedBy ECO_0000203 NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.
- befree-2016 importedOn "2016-02-19" NP561231.RAn739uxk6kGCpRqfKct9ZPMr_YEIDniQcCZiyl9r5L-4130_provenance.