Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_assertion type Assertion NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_head.
- NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_assertion description "[Multiple system atrophy (MSA) is a rare neurodegenerative disease of undetermined cause manifesting with progressive autonomic failure (AF), cerebellar ataxia and parkinsonism due to neuronal loss in multiple brain areas associated with (oligodendro)glial cytoplasmic alpha-synuclein (alpha SYN) inclusions (GCIs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.
- NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_assertion evidence source_evidence_literature NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.
- NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_assertion SIO_000772 20493840 NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.
- NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_assertion wasDerivedFrom befree-2016 NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.
- NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_assertion wasGeneratedBy ECO_0000203 NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.