Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion description "[Dopa-responsive dystonia (DRD), also known as Segawa syndrome or hereditary progressive dystonia with diurnal fluctuation, is clinically characterized by the occurrence of simultaneous or late Parkinsonism and by an excellent response to treatment with low doses of L-dopa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion evidence source_evidence_literature NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion SIO_000772 18752196 NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion wasDerivedFrom befree-2016 NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_assertion wasGeneratedBy ECO_0000203 NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.
- befree-2016 importedOn "2016-02-19" NP690037.RAWL8TFUQJ767JGUJMlVTmqCDuUFaN7eWzqneteQF-3B8130_provenance.