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Namespace Prefixes

PrefixIRI
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n3http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
dchttp://purl.org/dc/elements/1.1/
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
_:vb50943286
rdf:type
owl:Axiom
wdrs:describedby
n6:doid.owl
dc:type
n3:ECO_0007645
owl:annotatedProperty
n3:IAO_0000115
owl:annotatedSource
n3:DOID_0110597
owl:annotatedTarget
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, recurrent respiratory infections, persistent rhinosinusitis, otitis media, chronic cough, variable presence of situs abnormalities, and has_material_basis_in homozygous or compound heterozygous mutation in the ZMYND10 gene on chromosome 3p21.
obo:hasDbXref
url:https://www.ncbi.nlm.nih.gov/pubmed/23891471 url:https://www.ncbi.nlm.nih.gov/pubmed/23891469