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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_0090064
rdf:type
owl:Class
rdfs:subClassOf
n3:DOID_0090061 _:vb50942192 n3:DOID_0050736
rdfs:label
familial cold autoinflammatory syndrome 3
wdrs:describedby
n7:doid.owl
obo:id
DOID:0090064
obo:hasDbXref
OMIM:614468 ICD10CM:L50.2 ORDO:300359
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A familial cold autoinflammatory syndrome characterized by autosomal dominant inheritance of development of cutaneous urticaria, erythema and pruritus in response to cold exposure with. FCAS3 has_material_basis_in heterozygous deletion within the PLCG2 gene on chromosome 16q.
Subject Item
_:vb50942192
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000147
wdrs:describedby
n7:doid.owl