SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
n6 https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2 http://purl.obolibrary.org/obo/
wdrs http://www.w3.org/2007/05/powder-s#
rdfs http://www.w3.org/2000/01/rdf-schema#
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 n2:DOID_0080258
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0060655
_:vb50940650
rdfs:label
autosomal recessive congenital ichthyosis 14
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n6:doid.owl
obo:id
DOID:0080258
obo:hasDbXref
OMIM:617571
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An autosomal recessive congenital ichthyosis that is characterized by lamellar ichthyosis, ectropion, eclabium and hyperkeratosis that has_material_basis_in homozygous or compound heterozygous mutation in the SULT2B1 gene on chromosome 19q13.
Subject Item _:vb50940650
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n2:HP_0001197
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