<http://purl.obolibrary.org/obo/DOID_0110975>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110975>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050581> .
<http://purl.obolibrary.org/obo/DOID_0110975>	<http://www.w3.org/2000/01/rdf-schema#label>	"brachydactyly type B2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110975>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110975"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110975>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q73.8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110975>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A brachydactyly characterized by hypoplasia/aplasia of distal phalanges, distal symphalangism, fusion of carpal/tarsal bones, and partial cutaneous syndactyly that has_material_basis_in mutations in the NOG gene on chromosome 17q22."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110975>	<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_0110975>	<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_0110975>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"BDB2"@en .
<http://purl.obolibrary.org/obo/DOID_0110975>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:140908"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110975>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:611377"^^<http://www.w3.org/2001/XMLSchema#string> .