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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_0111028
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_2352 _:vb50944076
rdfs:label
hemochromatosis type 4
wdrs:describedby
n6:doid.owl
obo:id
DOID:0111028
obo:hasDbXref
OMIM:606069 UMLS_CUI:C1853733 GARD:10094 SNOMEDCT_US_2021_09_01:719975002 MESH:C537249 ORDO:139491
obo:hasExactSynonym
HFE4 autosomal dominant hereditary hemochromatosis ferroportin disease hemochromatosis due to defect in ferroportin
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32.
Subject Item
_:vb50944076
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:SO_0001537
wdrs:describedby
n6:doid.owl