Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_assertion wasGeneratedBy ECO_0000203 NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_assertion wasDerivedFrom befree-20150227 NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_assertion SIO_000772 8755644 NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_assertion evidence source_evidence_literature NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.
- NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_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." NP228424.RAT_2PfChWbM7CwVbyO56hgZ80NKZDRPYvPhh6FHYfnKU130_provenance.