This HTML5 document contains 18 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n5	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_0060065

rdf:type

owl:Class

rdfs:subClassOf

_:vb50938175 n2:DOID_0050737 n2:DOID_8955

rdfs:label

autosomal recessive pyridoxine-refractory sideroblastic anemia 2

rdfs:comment

OMIM mapping confirmed by DO. [LS].

wdrs:describedby

n5:doid.owl

obo:id

DOID:0060065

obo:hasDbXref

OMIM:205950

obo:hasExactSynonym

pyridoxine-refractory autosomal recessive sideroblastic anaemia pyridoxine-refractory autosomal recessive sideroblastic anemia autosomal recessive pyridoxine-refractory sideroblastic anaemia 2

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

A sideroblastic anemia that is characterized by microcytic hypochromic anemia and iron overload, and has_material_basis_in autosomal recessive inheritance of mutation in the SLC25A38 gene.

Subject Item

_:vb50938175

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000148

wdrs:describedby

n5:doid.owl