Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_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." NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_assertion evidence source_evidence_literature NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_assertion SIO_000772 16865326 NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_assertion wasDerivedFrom befree-20150227 NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_assertion wasGeneratedBy ECO_0000203 NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP967272.RAwdhyP7Zf4mjMeWaIVVHWE7j90caFk5mFi0JK__dYtdc130_provenance.