<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:6859"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:633"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:262500"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50956584	<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_9521>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:9521"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E34.3"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0271568"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
_:vb50956584	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_9521>	<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_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D046150"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50956584	<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_9521>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Laron-type isolated somatotropin defect"@en .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.w3.org/2000/01/rdf-schema#label>	"Laron syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C130994"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50956584 .
_:vb50956584	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:38196001"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_225> .
<http://purl.obolibrary.org/obo/DOID_9521>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndrome characterized by marked short stature with normal or high serum growth hormone and low serum insulin-like growth factor-1 levels that has_material_basis_in homozygous or compound heterozygous mutation in GHR on chromosome 5p13-p12."^^<http://www.w3.org/2001/XMLSchema#string> .