Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_assertion description "[We describe 2 patients whose clinical features resembled those of multiple system atrophy of the cerebellar subtype (MSA-C) but without ocular motor apraxia and hypoalbuminemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_assertion evidence source_evidence_literature NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_assertion SIO_000772 17049295 NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_assertion wasDerivedFrom befree-20150227 NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_assertion wasGeneratedBy ECO_0000203 NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP756913.RA-NSnuumrMKQaVqJbNpo0V-Z21zv--3j1pOAstJw9sX0130_provenance.