Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- 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.
- NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_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." NP1108758.RANa4rMNbXVP_GBlSlSw1Ldpo2_xOB9P58p9_rTF5jf7E130_provenance.