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DESCRIBE <http://purl.uniprot.org/SHA-384/9983B6298570A86D6EFB616B835193EA1B20AFABBC1F0F955ACE3C7BACC6C566726423672E64BF34659DCE0F8AEC009E>
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http://purl.uniprot.org/SHA-384/9983B6298570A86D6EFB616B835193EA1B20AFABBC1F0F955ACE3C7BACC6C566726423672E64BF34659DCE0F8AEC009E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9983B6298570A86D6EFB616B835193EA1B20AFABBC1F0F955ACE3C7BACC6C566726423672E64BF34659DCE0F8AEC009E
http://www.w3.org/2000/01/rdf-schema#comment
"In this study we sought to clarify the detailed mutational spectrum clinical features and genotype-phenotype correlations for ACTG1 gene associated autosomal dominant sensorineural hearing loss"
xsd:string
http://purl.uniprot.org/uniprot/#_4323FA0F869D3E65E81CFD9867E2E91FAB2D34496F3439A278FCFB510E9F19616A35AB7AE2C5B5B4BC8004D21D2A87B9
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9983B6298570A86D6EFB616B835193EA1B20AFABBC1F0F955ACE3C7BACC6C566726423672E64BF34659DCE0F8AEC009E
http://purl.uniprot.org/uniprot/Q9BTD2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9983B6298570A86D6EFB616B835193EA1B20AFABBC1F0F955ACE3C7BACC6C566726423672E64BF34659DCE0F8AEC009E
http://purl.uniprot.org/uniprot/#_Q9BTD2-mappedCitation-25792668
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9983B6298570A86D6EFB616B835193EA1B20AFABBC1F0F955ACE3C7BACC6C566726423672E64BF34659DCE0F8AEC009E