Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_assertion evidence source_evidence_literature NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_assertion SIO_000772 9648840 NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_assertion wasDerivedFrom befree-20150227 NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_assertion wasGeneratedBy ECO_0000203 NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.