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Namespace Prefixes

PrefixIRI
n3https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n6http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
dchttp://purl.org/dc/elements/1.1/
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
_:vb50951643
rdf:type
owl:Axiom
wdrs:describedby
n3:doid.owl
dc:type
n6:ECO_0007637 n6:ECO_0007638 n6:ECO_0007636
owl:annotatedProperty
n6:IAO_0000115
owl:annotatedSource
n6:DOID_3191
owl:annotatedTarget
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.
obo:hasDbXref
url:http://ghr.nlm.nih.gov/condition/nemaline-myopathy url:https://www.rarediseases.org/rare-disease-information/rare-diseases/byID/151/viewAbstract url:http://en.wikipedia.org/wiki/Nemaline_myopathy