This HTML5 document contains 23 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n6https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://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
n2:DOID_0110916
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_12971 n2:DOID_0050736 n2:DOID_0050737 _:vb50943902 _:vb50943903
rdfs:label
hereditary spherocytosis type 1
wdrs:describedby
n6:doid.owl
obo:id
DOID:0110916
obo:hasDbXref
OMIM:182900
obo:hasExactSynonym
hereditary spherocytosis 1 HS1 SPH1
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of ANK1 on chromosome 8p11.21.
Subject Item
_:vb50943902
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n6:doid.owl
Subject Item
_:vb50943903
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n6:doid.owl