Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_assertion description "[This study demonstrates the use of LV encoding mutant ataxin-3 to produce a model of MJD and brings evidence of striatal pathology, suggesting that this region may contribute to dystonia and chorea observed in some MJD patients and may represent a target for therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_assertion evidence source_evidence_literature NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_assertion SIO_000772 18385100 NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_assertion wasDerivedFrom befree-20150227 NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_assertion wasGeneratedBy ECO_0000203 NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557320.RAOcJhD-FKACgMBU9UVOYNBu90Ew62yGjrLQu9tg50NHc130_provenance.