SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
n4 https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n6 http://purl.obolibrary.org/obo/
wdrs http://www.w3.org/2007/05/powder-s#
dc http://purl.org/dc/elements/1.1/
obo http://www.geneontology.org/formats/oboInOwl#
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 _:vb50953087
rdf:type
owl:Axiom
wdrs:describedby
n4:doid.owl
dc:type
n6:ECO_0007637
n6:ECO_0007638
owl:annotatedProperty
n6:IAO_0000115
owl:annotatedSource
n6:DOID_4535
owl:annotatedTarget
A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles.
obo:hasDbXref
url:http://ghr.nlm.nih.gov/condition/autosomal-recessive-hypotrichosis
url:http://en.wikipedia.org/wiki/Hypotrichosis