Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_assertion> ?p ?o ?g. }
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- NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_assertion type Assertion NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_head.
- NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_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." NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_provenance.
- NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_assertion evidence source_evidence_literature NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_provenance.
- NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_assertion SIO_000772 15260953 NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_provenance.
- NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_assertion wasDerivedFrom befree-20140225 NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_provenance.
- NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_assertion wasGeneratedBy ECO_0000203 NP655488.RA8faqJrSoU91hN1BYHH6wF_LxXXBP_7s7TIQpqQdtHcg130_provenance.