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DESCRIBE <http://purl.uniprot.org/SHA-384/05E6FAF318A1153CF3F3DECBCFB995AD32F7E48014195FC5FEC786D94DD2F9690E153ECE7FFB2787380F0DEE8B1C1146>
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http://purl.uniprot.org/SHA-384/05E6FAF318A1153CF3F3DECBCFB995AD32F7E48014195FC5FEC786D94DD2F9690E153ECE7FFB2787380F0DEE8B1C1146
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/05E6FAF318A1153CF3F3DECBCFB995AD32F7E48014195FC5FEC786D94DD2F9690E153ECE7FFB2787380F0DEE8B1C1146
http://www.w3.org/2000/01/rdf-schema#comment
"A novel ATP1A2 heterozygous missense mutation found in a family with multicase Alternating hemiplegia of childhood."
xsd:string
http://purl.uniprot.org/uniprot/#_2F67C438C2CC7B4C2D84979D22EC5D7EDEC248F40B3407F8F6904DC1EF1EE2C6C2B5E0EC3D213090173C01AE04543FBF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/05E6FAF318A1153CF3F3DECBCFB995AD32F7E48014195FC5FEC786D94DD2F9690E153ECE7FFB2787380F0DEE8B1C1146
http://purl.uniprot.org/uniprot/B3KW93
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/05E6FAF318A1153CF3F3DECBCFB995AD32F7E48014195FC5FEC786D94DD2F9690E153ECE7FFB2787380F0DEE8B1C1146
http://purl.uniprot.org/uniprot/#_B3KW93-mappedCitation-15286158
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/05E6FAF318A1153CF3F3DECBCFB995AD32F7E48014195FC5FEC786D94DD2F9690E153ECE7FFB2787380F0DEE8B1C1146