Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP915538.RAfThTkpt49Vy-0lBfTVXjWgZM8ysFs--_8T7yr4EjZac130_provenance.