This HTML5 document contains 24 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_0111397
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0111396 n2:DOID_0050737 _:vb50944736 _:vb50944737
rdfs:label
congenital dyserythropoietic anemia type Ib
wdrs:describedby
n5:doid.owl
obo:id
DOID:0111397
obo:hasDbXref
MESH:D000742 SNOMEDCT_US_2021_09_01:59548005 OMIM:615631 UMLS_CUI:C0271933
obo:hasExactSynonym
CDAN1B CDA, type Ib
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in C15orf41 on chromosome 15q14.
Subject Item
_:vb50944736
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50944737
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:HP_0001197
wdrs:describedby
n5:doid.owl