This HTML5 document contains 20 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n6	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#
n4	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_0060196

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_332

rdfs:label

amyotrophic lateral sclerosis type 4

wdrs:describedby

n6:doid.owl

obo:id

DOID:0060196

obo:created_by

emitraka

obo:creation_date

2014-09-16T13:49:59Z

obo:hasDbXref

GARD:10502 ORDO:357043 OMIM:602433 ICD10CM:G12.2

obo:hasExactSynonym

distal hereditary motor neuropathy with pyramidal features ALS 4 dHMN with upper motor neuron signs amyotrophic lateral sclerosis 4, juvenile distal hereditary motor neuropathy with upper motor neuron signs amyotrophic lateral sclerosis 4

obo:hasOBONamespace

disease_ontology

obo:inSubset

n4:DO_rare_slim

n2:IAO_0000115

An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9.