Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_assertion> ?p ?o ?g. }
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- NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_assertion type Assertion NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_head.
- NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_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." NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_provenance.
- NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_assertion evidence source_evidence_literature NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_provenance.
- NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_assertion SIO_000772 15260953 NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_provenance.
- NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_assertion wasDerivedFrom befree-20150227 NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_provenance.
- NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_assertion wasGeneratedBy ECO_0000203 NP256129.RAH2Q7AIR5obaxThE0gO_CEwmT5wrnGAW9yrQlUQqVei8130_provenance.