<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_417> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942118	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"cryopyrin-associated periodic syndrome 3"@en .
_:vb50942118	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:607115"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.w3.org/2000/01/rdf-schema#label>	"CINCA Syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"IOMID syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0090029"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942118	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E85.0"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"chronic neurologic cutaneous and articular syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:1451"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"chronic infantile neurological cutaneous articular syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Prieur-Griscelli syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"NOMID syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50942118 .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"infantile-onset multisystem inflammatory disease"@en .
_:vb50942118	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0090029>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"neonatal-onset multisystem inflammatory disease"@en .