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- NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_assertion type Assertion NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_head.
- NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_assertion wasGeneratedBy ECO_0000203 NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.
- NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_assertion wasDerivedFrom befree-20140225 NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.
- NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_assertion SIO_000772 8734807 NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.
- NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_assertion evidence source_evidence_literature NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_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.