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- source_evidence_literature type ECO_0000212 NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP813973.RASF354us6FVkSi3B5PZusFoA6y-8cJ_geKRMLxJfua2I130_provenance.