Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_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." NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_assertion evidence source_evidence_literature NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_assertion SIO_000772 19815446 NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_assertion wasDerivedFrom befree-20140225 NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_assertion wasGeneratedBy ECO_0000203 NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614939.RAkNKf2eOa6BzbOqV8oYNVtY_doKbUa91wQ2JtGdQrXhY130_provenance.