Matches in Nanopublications for { ?s ?p "[Glycogen storage disease type Ia (GSD Ia, von Gierke disease) is an autosomal recessive inborn error of metabolism caused by the deficiency of D-glucose-6-phosphatase (G6Pase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion description "[Glycogen storage disease type Ia (GSD Ia, von Gierke disease) is an autosomal recessive inborn error of metabolism caused by the deficiency of D-glucose-6-phosphatase (G6Pase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_provenance.
- NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_assertion description "[Glycogen storage disease type Ia (GSD Ia, von Gierke disease) is an autosomal recessive inborn error of metabolism caused by the deficiency of D-glucose-6-phosphatase (G6Pase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.