Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_assertion> ?p ?o ?g. }
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- NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_assertion type Assertion NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_head.
- NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_assertion wasGeneratedBy ECO_0000203 NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_provenance.
- NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_assertion wasDerivedFrom befree-20140225 NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_provenance.
- NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_assertion SIO_000772 8755644 NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_provenance.
- NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_assertion evidence source_evidence_literature NP511295.RAb2bNVSUaXr8BgAKWO6P-2v4dsFwZt5vRzQKO8hnverE130_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.