Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_assertion> ?p ?o ?g. }
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- NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_assertion type Assertion NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_head.
- NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_assertion description "[Glycogen storage disease type Ia (GSD Ia; OMIM 232200) is an autosomal recessive disorder of glycogen metabolism caused by a deficiency of the microsomal glucose-6-phosphatase (G6Pase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_provenance.
- NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_assertion evidence source_evidence_literature NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_provenance.
- NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_assertion SIO_000772 18008183 NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_provenance.
- NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_assertion wasDerivedFrom befree-2016 NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_provenance.
- NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_assertion wasGeneratedBy ECO_0000203 NP640750.RAcNziz-D1N7JEq2Z1aNoiYe7GwWdWeaBGsflAbLjPnxQ130_provenance.