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DESCRIBE <http://purl.uniprot.org/SHA-384/96A8BE1D97AC0BD18C8B8D8C37B1E26CB129E5A4BE0C9CEC83CF301D544BBB99779E7A058B55CC077582C1345465204A>
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http://purl.uniprot.org/SHA-384/96A8BE1D97AC0BD18C8B8D8C37B1E26CB129E5A4BE0C9CEC83CF301D544BBB99779E7A058B55CC077582C1345465204A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/96A8BE1D97AC0BD18C8B8D8C37B1E26CB129E5A4BE0C9CEC83CF301D544BBB99779E7A058B55CC077582C1345465204A
http://www.w3.org/2000/01/rdf-schema#comment
"We studied four members of a family suffering from typical attacks of familial hemiplegic migraine (FHM) caused by a new mutation R548C of ATP1A2 gene in exon 12."
xsd:string
http://purl.uniprot.org/uniprot/#_3C972A001C0B60262C69F5666900351CB5711395253D1900B6DD2CABA7C98C5BC69F8608CBA9D9C28A815005CEB51BEE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/96A8BE1D97AC0BD18C8B8D8C37B1E26CB129E5A4BE0C9CEC83CF301D544BBB99779E7A058B55CC077582C1345465204A
http://purl.uniprot.org/uniprot/A0A0S2Z3W6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/96A8BE1D97AC0BD18C8B8D8C37B1E26CB129E5A4BE0C9CEC83CF301D544BBB99779E7A058B55CC077582C1345465204A
http://purl.uniprot.org/uniprot/#_A0A0S2Z3W6-mappedCitation-18498390
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/96A8BE1D97AC0BD18C8B8D8C37B1E26CB129E5A4BE0C9CEC83CF301D544BBB99779E7A058B55CC077582C1345465204A