<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060237> .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.w3.org/2000/01/rdf-schema#label>	"Warburg micro syndrome 4"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110719>	<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_0110719>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110719"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:615663"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q87.0"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the TBC1D20 gene on chromosome 20p13."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"WARBM4"@en .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Micro Syndrome 4"@en .
<http://purl.obolibrary.org/obo/DOID_0110719>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .