Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_assertion description "[Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_assertion evidence source_evidence_literature NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_assertion SIO_000772 7847376 NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_assertion wasDerivedFrom befree-2016 NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_assertion wasGeneratedBy ECO_0000203 NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.