Matches in Nanopublications for { ?s ?p "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_provenance.
- NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_provenance.
- NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_provenance.
- NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_provenance.
- NP1355444.RA3ibA7aidJxqjZ0UWGDZbLXbKAFMYUz2H1EoVYdjZBYo130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1355444.RA3ibA7aidJxqjZ0UWGDZbLXbKAFMYUz2H1EoVYdjZBYo130_provenance.