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http://purl.uniprot.org/SHA-384/49DA835E43909DC664AACEF070168C7C9E43A02C3093515503E8A336C3D495F994FBF692BDD1570230BD37BE845C759Chttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/49DA835E43909DC664AACEF070168C7C9E43A02C3093515503E8A336C3D495F994FBF692BDD1570230BD37BE845C759Chttp://www.w3.org/2000/01/rdf-schema#comment"The clinical diagnosis was confirmed by detection of compound heterozygous mutations in SBDS using whole-exome sequencing: a recurrent intronic mutation causing aberrant splicing (c.258+2T>C) and a novel missense variant in a highly conserved codon (c.41A>G p.Asn14Ser) considered to be damaging for the protein structure by in silico prediction programs"xsd:string
http://purl.uniprot.org/uniprot/#_2FD2A729795B0889B77057429FF37D91DDCE90902ABC007E731E0553B498A827290824B107C9797ECED59EBF2B82D687http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/49DA835E43909DC664AACEF070168C7C9E43A02C3093515503E8A336C3D495F994FBF692BDD1570230BD37BE845C759C
http://purl.uniprot.org/uniprot/Q9Y3A5http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/49DA835E43909DC664AACEF070168C7C9E43A02C3093515503E8A336C3D495F994FBF692BDD1570230BD37BE845C759C
http://purl.uniprot.org/uniprot/#_Q9Y3A5-mappedCitation-26866830http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/49DA835E43909DC664AACEF070168C7C9E43A02C3093515503E8A336C3D495F994FBF692BDD1570230BD37BE845C759C