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Namespace Prefixes

PrefixIRI
n6https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0080082
rdf:type
owl:Class
rdfs:subClassOf
_:vb50940348 _:vb50940349 n2:DOID_0050737 n2:DOID_0080683
rdfs:label
nonsyndromic congenital nail disorder 4
wdrs:describedby
n6:doid.owl
obo:id
DOID:0080082
obo:created_by
lschriml
obo:creation_date
2015-11-09T15:18:20Z
obo:hasAlternativeId
DOID:0050643
obo:hasDbXref
OMIM:206800 GARD:12930 MESH:C536377
obo:hasExactSynonym
HYPONYCHIA CONGENITA anonychia congenita
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A nonsyndromic congenital nail disorder that is characterized by complete absence or severe hypoplasia of all fingernails and toenails without significant bone anomalies, and that has_material_basis_in homozygous or compound heterozygous mutation in the R-spondin-4 gene on chromosome 20p13.
Subject Item
_:vb50940348
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n6:doid.owl
Subject Item
_:vb50940349
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:HP_0001197
wdrs:describedby
n6:doid.owl