This HTML5 document contains 32 embedded RDF statements represented using HTML+Microdata notation.

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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_0090024
rdf:type
owl:Class
rdfs:subClassOf
n4:DOID_0090020 _:vb50942088 _:vb50942089 n4:DOID_0050737
rdfs:label
split hand-foot malformation 1 with sensorineural hearing loss
wdrs:describedby
n3:doid.owl
obo:id
DOID:0090024
obo:hasDbXref
ORDO:71271 ICD10CM:Q87.2 OMIM:220600
obo:hasExactSynonym
SHFM1D congenital deafness with split hands and feet
obo:hasOBONamespace
disease_ontology
n4:IAO_0000115
A split-hand/foot malformation characterized by split-hand/foot malformation and sensorineural hearing impairment that has_material_basis_in homozygous mutation in the DLX5 gene on chromosome 7q21.
Subject Item
_:vb50942088
rdf:type
owl:Restriction
owl:onProperty
n4:IDO_0000664
owl:someValuesFrom
n4:GENO_0000148
wdrs:describedby
n3:doid.owl
Subject Item
_:vb50942089
rdf:type
owl:Restriction
owl:onProperty
n4:RO_0004026
owl:someValuesFrom
_:vb50942090
wdrs:describedby
n3:doid.owl
Subject Item
_:vb50942090
rdf:type
owl:Class
owl:intersectionOf
_:vb50942092
wdrs:describedby
n3:doid.owl
Subject Item
_:vb50942091
rdf:first
n4:UBERON_0002398
rdf:rest
rdf:nil
wdrs:describedby
n3:doid.owl
Subject Item
_:vb50942092
rdf:first
n4:UBERON_0002387
rdf:rest
_:vb50942091
wdrs:describedby
n3:doid.owl