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DESCRIBE <http://purl.uniprot.org/SHA-384/836EE7A3B7121221A27C6DD7FB10597D30670E1560157151B82925F63527A73DA6454BF0AC1CF94EED885B2FB52299AF>
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http://purl.uniprot.org/SHA-384/836EE7A3B7121221A27C6DD7FB10597D30670E1560157151B82925F63527A73DA6454BF0AC1CF94EED885B2FB52299AF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/836EE7A3B7121221A27C6DD7FB10597D30670E1560157151B82925F63527A73DA6454BF0AC1CF94EED885B2FB52299AF
http://www.w3.org/2000/01/rdf-schema#comment
"The discovery of this new ALB mutation sheds light on the molecular mechanism underlying the analbuminemic trait and may serve in the development of a rapid genetic test for the identification of a-symptomatic heterozygous carriers."
xsd:string
http://purl.uniprot.org/uniprot/#_06B8A9622A4CA00B03E1E5A18502D72A740EA5F3BBC6B87AD1E23D0A2744B82A4CDBFDABDBEDD27CCB05E76852E6C3D9
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/836EE7A3B7121221A27C6DD7FB10597D30670E1560157151B82925F63527A73DA6454BF0AC1CF94EED885B2FB52299AF
http://purl.uniprot.org/uniprot/Q56G89
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/836EE7A3B7121221A27C6DD7FB10597D30670E1560157151B82925F63527A73DA6454BF0AC1CF94EED885B2FB52299AF
http://purl.uniprot.org/uniprot/#_Q56G89-mappedCitation-23176518
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/836EE7A3B7121221A27C6DD7FB10597D30670E1560157151B82925F63527A73DA6454BF0AC1CF94EED885B2FB52299AF