This HTML5 document contains 24 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n8https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
skoshttp://www.w3.org/2004/02/skos/core#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
n4http://purl.obolibrary.org/obo/doid#
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_332
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_231
rdfs:label
amyotrophic lateral sclerosis
skos:exactMatch
MESH:D000690
wdrs:describedby
n8:doid.owl
obo:id
DOID:332
obo:hasDbXref
NCI:C34373 SNOMEDCT_US_2021_09_01:86044005 ICD10CM:G12.21 EFO:0000253 ORDO:803 KEGG:05014 GARD:5786 MESH:D000690 UMLS_CUI:C0002736 OMIM:PS105400 ICD9CM:335.20
obo:hasExactSynonym
motor neuron disease, bulbar ALS Lou Gehrig's disease
obo:hasOBONamespace
disease_ontology
obo:inSubset
n4:DO_FlyBase_slim n4:NCIthesaurus
n2:IAO_0000115
A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.