<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym>	"Fragilitas ossium"@en .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:12347"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:756.51"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D010013"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasAlternativeId>	"DOID:14708"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<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_12347>	<http://www.w3.org/2000/01/rdf-schema#comment>	"Xref MGI.\nOMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.w3.org/2000/01/rdf-schema#label>	"osteogenesis imperfecta"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Vrolik's disease"@en .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q78.0"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"brittle bone disease"@en .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:1017"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Lobstein's syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_12347>	<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_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C26837"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An osteochondrodysplasia that has_material_basis_in a deficiency in type-I collagen which results_in brittle bones and defective connective tissue."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_2256> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0029434"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:254109004"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Osteopsathyrosis"@en .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:PS166200"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12347>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:666"^^<http://www.w3.org/2001/XMLSchema#string> .