Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_assertion> ?p ?o ?g. }
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- NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_assertion type Assertion NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_head.
- NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_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." NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.
- NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_assertion evidence source_evidence_literature NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.
- NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_assertion SIO_000772 20493840 NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.
- NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_assertion wasDerivedFrom befree-20150227 NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.
- NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_assertion wasGeneratedBy ECO_0000203 NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.