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DESCRIBE <http://purl.uniprot.org/SHA-384/EBE99512DB024350F12BE36142BADA792A68C199A3791EBA89BCC5D5800A7854C1F1FBBEB03B07B7D98F2A75B2D4D6DA>
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http://purl.uniprot.org/SHA-384/EBE99512DB024350F12BE36142BADA792A68C199A3791EBA89BCC5D5800A7854C1F1FBBEB03B07B7D98F2A75B2D4D6DA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EBE99512DB024350F12BE36142BADA792A68C199A3791EBA89BCC5D5800A7854C1F1FBBEB03B07B7D98F2A75B2D4D6DA
http://www.w3.org/2000/01/rdf-schema#comment
"Genetic examinations of the SCN5A gene at 6 positive patients showed 6 known polymorphisms 8 new single nucleotide point (SNP) variants located at exons and 12 new single nucleotide point variants located at introns"
xsd:string
http://purl.uniprot.org/uniprot/#_D9C01DF5C4C9FC50BB2969895B6EF00B4191FA1672AD8FEB0F553A006F67AE48C1F26D58AF1270975C033068419BD445
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EBE99512DB024350F12BE36142BADA792A68C199A3791EBA89BCC5D5800A7854C1F1FBBEB03B07B7D98F2A75B2D4D6DA
http://purl.uniprot.org/uniprot/H9KVD2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EBE99512DB024350F12BE36142BADA792A68C199A3791EBA89BCC5D5800A7854C1F1FBBEB03B07B7D98F2A75B2D4D6DA
http://purl.uniprot.org/uniprot/#_H9KVD2-mappedCitation-25401102
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EBE99512DB024350F12BE36142BADA792A68C199A3791EBA89BCC5D5800A7854C1F1FBBEB03B07B7D98F2A75B2D4D6DA