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http://purl.uniprot.org/SHA-384/98E6D41CCB89D9CD51F83665A97FE2B623D4511A1A2EEB23C423B88954C3E27C8507E05EBDB8B7BE751CFB42F38CEC31http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/98E6D41CCB89D9CD51F83665A97FE2B623D4511A1A2EEB23C423B88954C3E27C8507E05EBDB8B7BE751CFB42F38CEC31http://www.w3.org/2000/01/rdf-schema#comment"Data suggest that the following genetic modifications are involved in neonatal diabetes mellitus patients in Oman: (1) mutation in KCNJ11 (potassium voltage-gated channel subfamily J member 11; one patient); (2) mutation in GCK (glucokinase); (3) mutation in SLC2A2 (glucose transporter type 2); (4) chromosome 6q24 methylation abnormalities."xsd:string
http://purl.uniprot.org/uniprot/#_11C2B629F9B044F9A0F60A8234D417BBD2A9735310C81B6875109852A6C002266DA7219207212487F6501B4FBA9577BEhttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/98E6D41CCB89D9CD51F83665A97FE2B623D4511A1A2EEB23C423B88954C3E27C8507E05EBDB8B7BE751CFB42F38CEC31
http://purl.uniprot.org/uniprot/A7LFL1http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/98E6D41CCB89D9CD51F83665A97FE2B623D4511A1A2EEB23C423B88954C3E27C8507E05EBDB8B7BE751CFB42F38CEC31
http://purl.uniprot.org/uniprot/#_A7LFL1-mappedCitation-29329106http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/98E6D41CCB89D9CD51F83665A97FE2B623D4511A1A2EEB23C423B88954C3E27C8507E05EBDB8B7BE751CFB42F38CEC31