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DESCRIBE <http://purl.uniprot.org/SHA-384/03ABA60EE555229ED650308CD4A46C7048F45E7F20C47F98B3B7C5FC4FB3E8BA5B890756DF8B12D17B4D3CE53D581FEB>
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http://purl.uniprot.org/SHA-384/03ABA60EE555229ED650308CD4A46C7048F45E7F20C47F98B3B7C5FC4FB3E8BA5B890756DF8B12D17B4D3CE53D581FEB
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/03ABA60EE555229ED650308CD4A46C7048F45E7F20C47F98B3B7C5FC4FB3E8BA5B890756DF8B12D17B4D3CE53D581FEB
http://www.w3.org/2000/01/rdf-schema#comment
"Germline mosaicism for ATP1A3 mutations is a likely explanation for familial recurrence and should be considered during recurrence risk counseling for families of children with ATP1A3-related disorders."
xsd:string
http://purl.uniprot.org/uniprot/#_1D1AFED02959E57B94D8CBDFBDD49CB9B1DB909338E1C0F3ADFEBB0208478AFC4B957DC36962E76CB7E21FF3C9573DA5
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/03ABA60EE555229ED650308CD4A46C7048F45E7F20C47F98B3B7C5FC4FB3E8BA5B890756DF8B12D17B4D3CE53D581FEB
http://purl.uniprot.org/uniprot/Q58I21
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/03ABA60EE555229ED650308CD4A46C7048F45E7F20C47F98B3B7C5FC4FB3E8BA5B890756DF8B12D17B4D3CE53D581FEB
http://purl.uniprot.org/uniprot/#_Q58I21-mappedCitation-27726050
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/03ABA60EE555229ED650308CD4A46C7048F45E7F20C47F98B3B7C5FC4FB3E8BA5B890756DF8B12D17B4D3CE53D581FEB