This HTML5 document contains 25 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n7	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#
n8	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_3191

rdf:type

owl:Class

rdfs:subClassOf

_:vb50951642 n2:DOID_422

rdfs:label

nemaline myopathy

rdfs:comment

Xref MGI.

wdrs:describedby

n7:doid.owl

obo:id

DOID:3191

obo:hasDbXref

GARD:12033 ICD10CM:G71.21 OMIM:PS161800 SNOMEDCT_US_2021_09_01:75072002 UMLS_CUI:C0206157 MESH:D017696 ORDO:607

obo:hasExactSynonym

rod myopathy nemaline rod myopathy Nemaline body disease

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:DO_FlyBase_slim n8:DO_rare_slim

n2:IAO_0000115

A congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity; certain muscle fibers show the presence of rod-like structures called nemaline bodies.

Subject Item

_:vb50951642

rdf:type

owl:Restriction

owl:onProperty

n2:RO_0002452

owl:someValuesFrom

n2:SYMP_0000094

wdrs:describedby

n7:doid.owl