Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_assertion type Assertion NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_head.
- NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_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." NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_provenance.
- NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_assertion evidence source_evidence_literature NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_provenance.
- NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_assertion SIO_000772 15260953 NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_provenance.
- NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_assertion wasDerivedFrom befree-2016 NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_provenance.
- NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_assertion wasGeneratedBy ECO_0000203 NP452518.RASWmm53V7YscYqknj2mddqG9LU39Mk3dqw2nG_zmM_ok130_provenance.