<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.w3.org/2000/01/rdf-schema#label>	"nemaline myopathy"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"rod myopathy"@en .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:12033"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50951642	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000094> .
_:vb50951642	<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_3191>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_FlyBase_slim> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.w3.org/2000/01/rdf-schema#comment>	"Xref MGI."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:G71.21"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:3191"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50951642	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:PS161800"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50951642	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50951642 .
<http://purl.obolibrary.org/obo/DOID_3191>	<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_3191>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:75072002"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0206157"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D017696"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"nemaline rod myopathy"@en .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_422> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Nemaline body disease"@en .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:607"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3191>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity; certain muscle fibers show the presence of rod-like structures called nemaline bodies."^^<http://www.w3.org/2001/XMLSchema#string> .