This HTML5 document contains 26 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n5https://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_5112
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_5113 _:vb50953625 _:vb50953626 _:vb50953627
rdfs:label
copper deficiency myelopathy
wdrs:describedby
n5:doid.owl
obo:id
DOID:5112
obo:hasDbXref
UMLS_CUI:C0038981 SNOMEDCT_US_2021_09_01:78714004 MESH:D013540
obo:hasExactSynonym
human swayback
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A nutritional deficiency disease that is characterized by deficiency of copper, causing spastic gait and ataxia, often with anemia and neutropenia, has_symptom imbalance and jerking movements, and has_material_basis_in copper deficiency possibly due to malabsorption or excess zinc ingestion.
Subject Item
_:vb50953625
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:DOID_2355
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50953626
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000005
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50953627
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000318
wdrs:describedby
n5:doid.owl