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http://purl.uniprot.org/SHA-384/A11B5DA0C11EF344246B2D8D5ADAE7854346377769BF48BAEF527FD18A5CAC3808B7D8BECD8A9B8F82A94BE8261A508Fhttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A11B5DA0C11EF344246B2D8D5ADAE7854346377769BF48BAEF527FD18A5CAC3808B7D8BECD8A9B8F82A94BE8261A508Fhttp://www.w3.org/2000/01/rdf-schema#comment"study identified new nonsense and missense mutations in the EXOSC3 gene and showed mutations in this gene are exclusively found in pontocerebellar hypoplasia type 1 patients; there are evident genotype-phenotype correlations in EXOSC3-mediated PCH reflected in clinical outcome age of death and pons hypoplasia"xsd:string
http://purl.uniprot.org/uniprot/#_0EE789B03056F0B6554DE7CC49E614711A7CFB1D7920F00A4D7005B5FBA515A845900CD23EFB2EF6A7B6EBC400F7440Chttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/A11B5DA0C11EF344246B2D8D5ADAE7854346377769BF48BAEF527FD18A5CAC3808B7D8BECD8A9B8F82A94BE8261A508F
http://purl.uniprot.org/uniprot/Q9NYS3http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/A11B5DA0C11EF344246B2D8D5ADAE7854346377769BF48BAEF527FD18A5CAC3808B7D8BECD8A9B8F82A94BE8261A508F
http://purl.uniprot.org/uniprot/#_Q9NYS3-mappedCitation-24524299http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/A11B5DA0C11EF344246B2D8D5ADAE7854346377769BF48BAEF527FD18A5CAC3808B7D8BECD8A9B8F82A94BE8261A508F