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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_0111944
rdf:type
owl:Class
rdfs:subClassOf
_:vb50945787 n3:DOID_612 n3:DOID_0050737
rdfs:label
immunodeficiency 31B
wdrs:describedby
n7:doid.owl
obo:id
DOID:0111944
obo:hasDbXref
OMIM:613796 ORDO:391311
obo:hasExactSynonym
predisposition to severe viral infection due to STAT1 deficiency susceptibility to viral and mycobacterial infections due to STAT1 deficiency autosomal recessive immunodeficiency 31B, mycobacterial and viral infections IMD31B autosomal recessive STAT1 deficiency
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A primary immunodeficiency disease characterized by impaired cellular responses to interferons A, B, and G resulting increased susceptibility to mycobacteria, Salmonella, and viruses that has_material_basis_in homozygous or compound heterozygous mutation in STAT1 on chromosome 2q32.2.
Subject Item
_:vb50945787
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000148
wdrs:describedby
n7:doid.owl