<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"alpha thalassemia, haemoglobin H type"@en .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"alpha thalassemia, hemoglobin H type"@en .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:613978"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.w3.org/2000/01/rdf-schema#label>	"hemoglobin H disease"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:93616"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hemoglobin H disease, deletional"@en .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"alpha-thalassemia intermedia"@en .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110031"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:D56.0"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_1099> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"HBH"@en .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"haemoglobin H disease"@en .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0110031>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"haemoglobin H disease, deletional"@en .