This HTML5 document contains 16 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n8	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n6	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_0060719

rdf:type

owl:Class

rdfs:subClassOf

_:vb50939262 n2:DOID_0060655

rdfs:label

autosomal recessive congenital ichthyosis 10

wdrs:describedby

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obo:id

DOID:0060719

obo:hasDbXref

ICD10CM:Q80.2 OMIM:615024

obo:hasExactSynonym

ARCI10

obo:hasOBONamespace

disease_ontology

obo:inSubset

n6:DO_rare_slim

n2:IAO_0000115

An autosomal recessive congenital ichthyosis characterized by generalized ichthyosis, moderade erythroderma, palmoplantar keratoderma and hypergranulosis that has_material_basis_in homozygous mutation in the PNPLA1 gene on chromosome 6p21.

Subject Item

_:vb50939262

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owl:Restriction

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n2:RO_0004019

owl:someValuesFrom

n2:HP_0001197

wdrs:describedby

n8:doid.owl