This HTML5 document contains 19 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_0111941
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_612 _:vb50945781 n2:DOID_0050737
rdfs:label
immunodeficiency 20
wdrs:describedby
n6:doid.owl
obo:id
DOID:0111941
obo:hasDbXref
OMIM:615707 ORDO:437552
obo:hasExactSynonym
CD16 deficiency autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity IMD20 autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A primary immunodeficiency disease characterized by a defect in spontaneous NK cell cytotoxicity that has_material_basis_in homozygous or compound heterozygous mutation in FCGR3A on chromosome 1q23.3.
Subject Item
_:vb50945781
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n6:doid.owl