This HTML5 document contains 21 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3http://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
n3:DOID_0111163
rdf:type
owl:Class
rdfs:subClassOf
_:vb50944339 n3:DOID_0111165
rdfs:label
molybdenum cofactor deficiency type B
wdrs:describedby
n7:doid.owl
obo:id
DOID:0111163
obo:hasDbXref
ORDO:308393 UMLS_CUI:C1854989 OMIM:252160 SNOMEDCT_US_2021_09_01:1003368009 MESH:C565373
obo:hasExactSynonym
MOCODB molybdenum cofactor deficiency complementation group B combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B MOCOD type B
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11.
Subject Item
_:vb50944339
rdf:type
owl:Restriction
owl:onProperty
n3:RO_0004019
owl:someValuesFrom
n3:SO_0001537
wdrs:describedby
n7:doid.owl