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http://purl.uniprot.org/SHA-384/E2E1251A16E73AC3728B00DE7DEA269143001B23A8E32F4B848F5C626AF0CC49290ADA42509D8FCD4DDB5FEC7DE934B7http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E2E1251A16E73AC3728B00DE7DEA269143001B23A8E32F4B848F5C626AF0CC49290ADA42509D8FCD4DDB5FEC7DE934B7http://www.w3.org/2000/01/rdf-schema#comment"The prevalence of the majority of non-pathological genetic variations is similar in the Latvian ARVD-C patients and the European population. Possibly pathogenic variations were found only in 10% of our registry patients which could mean that PKP2 and DSG2 are not the most commonly affected genes in the Latvian population."xsd:string
http://purl.uniprot.org/uniprot/#_A1E1AF97527750416CDE702408850844FE1FB109217DD00334065AE19D18783B4B70ECF6D8DD635DDA42A0C23E2D495Fhttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/E2E1251A16E73AC3728B00DE7DEA269143001B23A8E32F4B848F5C626AF0CC49290ADA42509D8FCD4DDB5FEC7DE934B7
http://purl.uniprot.org/uniprot/Q14126http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/E2E1251A16E73AC3728B00DE7DEA269143001B23A8E32F4B848F5C626AF0CC49290ADA42509D8FCD4DDB5FEC7DE934B7
http://purl.uniprot.org/uniprot/#_Q14126-mappedCitation-30391969http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/E2E1251A16E73AC3728B00DE7DEA269143001B23A8E32F4B848F5C626AF0CC49290ADA42509D8FCD4DDB5FEC7DE934B7