Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_assertion description "[This contrasts with homozygous parkin, PINK1 or DJ1 parkinsonism, characterized by young-onset (usually <40 years), and a comparatively benign course of predominantly levodopa-responsive symptoms without dementia or prominent dysautonomia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_assertion evidence source_evidence_literature NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_assertion SIO_000772 19815446 NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_assertion wasDerivedFrom befree-2016 NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_assertion wasGeneratedBy ECO_0000203 NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP768307.RA8emDAQjfrxBPU9XugSYY27Uqy9I0v2Ysoo7bbXq5gjQ130_provenance.