Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_assertion> ?p ?o ?g. }
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- NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_assertion type Assertion NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_head.
- NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_assertion wasGeneratedBy ECO_0000218 NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_provenance.
- NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_assertion wasDerivedFrom ctd_human-20130708 NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_provenance.
- NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_assertion SIO_000772 8755644 NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_provenance.
- NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_assertion evidence source_evidence_curated NP7916.RASgy8b4cq5ig5J_mckFO-2votKWD6U12-89cGaSVlM6Q130_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.