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Namespace Prefixes

PrefixIRI
n7https://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_0060201
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_332
rdfs:label
amyotrophic lateral sclerosis type 10
wdrs:describedby
n7:doid.owl
obo:id
DOID:0060201
obo:created_by
emitraka
obo:creation_date
2014-09-16T14:36:54Z
obo:hasDbXref
GARD:10497 OMIM:612069
obo:hasExactSynonym
ALS10 amyotrophic lateral sclerosis 10 amyotrophic lateral sclerosis 10, with or without frontotemporal dementia TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TARDBP gene on chromosome 1.