_:vb50937339	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50937339	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007646> .
_:vb50937339	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50937339	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007645> .
_:vb50937339	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50937339	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007637> .
_:vb50937339	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007638> .
_:vb50937339	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A Cowden syndrome that is characterized by macrocephaly, multiple noncancerous tumors and hamartomas, and dark freckles on the penis, and has_material_basis_in heterozygous germline mutation in the PTEN gene on chromosome 10q23."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50937339	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.ncbi.nlm.nih.gov/pubmed/31062505"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50937339	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://ghr.nlm.nih.gov/condition/bannayan-riley-ruvalcaba-syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50937339	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0050657> .
_:vb50937339	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.ncbi.nlm.nih.gov/books/NBK1488/"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50937339	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://en.wikipedia.org/wiki/Bannayan%E2%80%93Riley%E2%80%93Ruvalcaba_syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .