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Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n3:DOID_0070220
rdf:type
owl:Class
rdfs:subClassOf
n3:DOID_13317 _:vb50939937
rdfs:label
familial hyperinsulinemic hypoglycemia 5
wdrs:describedby
n7:doid.owl
obo:id
DOID:0070220
obo:hasDbXref
ORDO:263458 OMIM:609968
obo:hasExactSynonym
hyperinsulinemic hypoglycemia due to insulin receptor deficiency hyperinsulinemic hypoglycemia due to INSR deficiency hyperinsulinism due to INSR deficiency HHF5
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postprandial hypoglycemia, fasting hyperinsulinemia, and an elevated serum insulin-to-C peptide ratio that has_material_basis_in mutation in the INSR gene on chromosome 19p13.
Subject Item
_:vb50939937
rdf:type
owl:Restriction
owl:onProperty
n3:RO_0004019
owl:someValuesFrom
n3:SO_0001537
wdrs:describedby
n7:doid.owl