Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_assertion> ?p ?o ?g. }
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- NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_assertion type Assertion NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_head.
- NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_assertion description "[All the subjects except for one family had typical manifestations of autosomal dominant GTPCH-I deficient DRD including early childhood onset dystonia predominantly in the legs, marked diurnal variation, intact cognition, no other systemic symptoms, and excellent sustained response to levodopa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_provenance.
- NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_assertion evidence source_evidence_literature NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_provenance.
- NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_assertion SIO_000772 24018121 NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_provenance.
- NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_assertion wasDerivedFrom befree-20150227 NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_provenance.
- NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_assertion wasGeneratedBy ECO_0000203 NP420645.RAwRv2a5-JDuT780YVYEwzZnl7uGaoEtM4VBFdOKQ9nfA130_provenance.