<http://purl.obolibrary.org/obo/DOID_0111631>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:617981"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111631>	<http://www.w3.org/2000/01/rdf-schema#label>	"familial erythrocytosis 7"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111631>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111631>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111631"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111631>	<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_0111631>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"alpha-globin type polycythemia"@en .
<http://purl.obolibrary.org/obo/DOID_0111631>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"ECYT7"@en .
<http://purl.obolibrary.org/obo/DOID_0111631>	<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_0111631>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_10780> .
<http://purl.obolibrary.org/obo/DOID_0111631>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A primary polycythemia characterized by high oxygen affinity hemoglobin and compensatory polycythemia that has_material_basis_in heterozygous mutation in either HBA2 or HBA1 on chromosome 16p13.3."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111631>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"alpha-globin type erythrocytosis"@en .