Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_assertion description "[Hyperinsulinism-hyperammonemia syndrome (HI/HA) (OMIM 606762), the second most common form of congenital hyperinsulinism (CHI) is associated with activating missense mutations in the GLUD1 gene, which encodes the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_assertion evidence source_evidence_literature NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_assertion SIO_000772 21932603 NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_assertion wasDerivedFrom befree-20140225 NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_assertion wasGeneratedBy ECO_0000203 NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP308558.RAeGe8kFYr4x-9N9ZCXsF_3TaYT6oNgIIJiO-BCfm1k8c130_provenance.