Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_assertion> ?p ?o ?g. }
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- NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_assertion type Assertion NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_head.
- NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_assertion wasGeneratedBy ECO_0000203 NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_provenance.
- NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_assertion wasDerivedFrom befree-2016 NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_provenance.
- NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_assertion SIO_000772 23462481 NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_provenance.
- NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_assertion evidence source_evidence_literature NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_provenance.
- NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_assertion description "[Mutations in seven genes are robustly associated with autosomal dominant (SNCA, LRRK2, EIF4G1, VPS35) or recessive (parkin/PARK2, PINK1, DJ1/PARK7) Parkinson's disease (PD) or parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057962.RAf5JeXVi0NU_n6xW55xBVcmnmHGAQMbpZg60L4qorzio130_provenance.