Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_assertion description "[Rapid-onset dystonia-parkinsonism (RDP, DYT12) is a distinctive autosomal-dominant movement disorder with variable expressivity and reduced penetrance characterized by abrupt onset of dystonia, usually accompanied by signs of parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_assertion evidence source_evidence_literature NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_assertion SIO_000772 15260953 NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_assertion wasDerivedFrom befree-20140225 NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_assertion wasGeneratedBy ECO_0000203 NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP642717.RA8UzbQ4PeWzK1Y8l4PdcQG9Lt06GbzusbnqtG0G1bfdE130_provenance.