<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_2121> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.w3.org/2000/01/rdf-schema#label>	"scalp-ear-nipple syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945034 .
_:vb50945034	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An ectodermal dysplasia characterized by cutis aplasia of the scalp, breast anomalies that range from hypothelia or athelia to amastia, and minor anomalies of the external ears that has_material_basis_in heterozygous mutation in KCTD1 on chromosome 18q11.2."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"SENS"@en .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples"@en .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:159"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945034	<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_0111550>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Sen Syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1867020"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945034	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50945034	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:181270"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:2036"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:721888002"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111550"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<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_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C536623"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Finlay-Marks syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0111550>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .