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http://purl.uniprot.org/SHA-384/2897F3826400E3EBEBB66A276B619B6E8E08DCB0D1B13E6717A192DECF9B21F872DFC5CB28C1B9313640202E1386C005http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2897F3826400E3EBEBB66A276B619B6E8E08DCB0D1B13E6717A192DECF9B21F872DFC5CB28C1B9313640202E1386C005http://www.w3.org/2000/01/rdf-schema#comment"IN TMD patients a novel locus at genome-wide level of significance (rs73460075 OR = 0.56 P = 3.8 x 10(-8)) in the intron of the dystrophin gene DMD (X chromosome) and a suggestive locus on chromosome 7 (rs73271865 P = 2.9 x 10(-7)) upstream of the Sp4 Transcription Factor ( SP4) gene were identified in the discovery cohort but neither of these was replicated."xsd:string
http://purl.uniprot.org/uniprot/#_EE9A15FBB506E9D698FEA52F5E38346436CF65931C210B58352B306E9E09F79222AAC153D1DB3A5ABF7457F823EC6661http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/2897F3826400E3EBEBB66A276B619B6E8E08DCB0D1B13E6717A192DECF9B21F872DFC5CB28C1B9313640202E1386C005
http://purl.uniprot.org/uniprot/Q02446http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/2897F3826400E3EBEBB66A276B619B6E8E08DCB0D1B13E6717A192DECF9B21F872DFC5CB28C1B9313640202E1386C005
http://purl.uniprot.org/uniprot/#_Q02446-mappedCitation-28081371http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/2897F3826400E3EBEBB66A276B619B6E8E08DCB0D1B13E6717A192DECF9B21F872DFC5CB28C1B9313640202E1386C005