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Namespace Prefixes

PrefixIRI
n3https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n4http://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
n4:DOID_0070166
rdf:type
owl:Class
rdfs:subClassOf
_:vb50939832 n4:DOID_0111910 n4:DOID_0050737
rdfs:label
spermatogenic failure 20
wdrs:describedby
n3:doid.owl
obo:id
DOID:0070166
obo:hasDbXref
OMIM:617593
obo:hasExactSynonym
SPGF20
obo:hasOBONamespace
disease_ontology
n4:IAO_0000115
A male infertility characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP44 gene on chromosome 3q13.
Subject Item
_:vb50939832
rdf:type
owl:Restriction
owl:onProperty
n4:IDO_0000664
owl:someValuesFrom
n4:GENO_0000148
wdrs:describedby
n3:doid.owl