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Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n5	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
dc	http://purl.org/dc/elements/1.1/
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

_:vb50951140

rdf:type

owl:Axiom

wdrs:describedby

n7:doid.owl

dc:type

n5:ECO_0007638 n5:ECO_0007646

owl:annotatedProperty

n5:IAO_0000115

owl:annotatedSource

n5:DOID_2749

owl:annotatedTarget

A glycogen storage disease that has_material_basis_in deficiency of the glucose-6-phosphatase enzyme which impairs the ability of the liver to produce free glucose from glycogen and from gluconeogenesis and is characterized by accumulation of glycogen and fat in the liver and kidneys, resulting in hepatomegaly and renomegaly.

obo:hasDbXref

url:http://en.wikipedia.org/wiki/Von_Gierke%27s_disease url:http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_I url:http://www.ncbi.nlm.nih.gov/books/NBK1312/