SPARQL
Downloads
Documentation/Help
Skip Header
Results
Your Query
Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/05E0FC9416507C1FC9ECA8C38750819CF0D6F03B0C54AE60D83A147697B3E22E7CCD94036F0550E8EA70F00902116D16>
Submit Query
Cancel
RDF/XML
NTriples
Turtle
Show query
Share
Subject
Predicate
Object
http://purl.uniprot.org/SHA-384/05E0FC9416507C1FC9ECA8C38750819CF0D6F03B0C54AE60D83A147697B3E22E7CCD94036F0550E8EA70F00902116D16
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/05E0FC9416507C1FC9ECA8C38750819CF0D6F03B0C54AE60D83A147697B3E22E7CCD94036F0550E8EA70F00902116D16
http://www.w3.org/2000/01/rdf-schema#comment
"The rsults of this study indicate the mutations cause severe phenotypesd of ATP1A3-related disorder spectrum that include catastrophic early life epilepsy episodic apnea and postnatal microcephaly."
xsd:string
http://purl.uniprot.org/uniprot/#_F25E25B9C79D209394D9AD7494B83AE17EE6EAAE5C7EEEF81E73F3CF02AA355D5D03F5F53194105FEA2755D9EF35A950
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/05E0FC9416507C1FC9ECA8C38750819CF0D6F03B0C54AE60D83A147697B3E22E7CCD94036F0550E8EA70F00902116D16
http://purl.uniprot.org/uniprot/B3KV59
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/05E0FC9416507C1FC9ECA8C38750819CF0D6F03B0C54AE60D83A147697B3E22E7CCD94036F0550E8EA70F00902116D16
http://purl.uniprot.org/uniprot/#_B3KV59-mappedCitation-25656163
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/05E0FC9416507C1FC9ECA8C38750819CF0D6F03B0C54AE60D83A147697B3E22E7CCD94036F0550E8EA70F00902116D16