Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP415075.RAp3EPWo2XBC6_j_f9SPwl7kHND7pOEfv5_6J9_T_-GfM130_provenance.