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http://purl.uniprot.org/SHA-384/1844B0E12E637B0C94FC9A1365B54EEC40853D112C1DD3E3B305146A0CE420C57B2F8670811B71B661451AC1EBC8D4E6http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1844B0E12E637B0C94FC9A1365B54EEC40853D112C1DD3E3B305146A0CE420C57B2F8670811B71B661451AC1EBC8D4E6http://www.w3.org/2000/01/rdf-schema#comment"Eligible patients for this study were healthy women with >/= 17% lifetime risk of breast cancer or with a mutation in BRCA1 or BRCA2. A total of 632 women were screened between 2002 and 2012 (each for 6 years). During the study 30 women were diagnosed with breast cancer with 10 of these diagnoses occurring between screening visits and six of the 10 diagnosed women were gene carriers"xsd:string
http://purl.uniprot.org/uniprot/#_8CF2B5050F76FFDDC8606B017E2EE2450264732ABC8BCABB83A951A947AEC6EE19771CDBFCC6E7071D811203BAAD4508http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/1844B0E12E637B0C94FC9A1365B54EEC40853D112C1DD3E3B305146A0CE420C57B2F8670811B71B661451AC1EBC8D4E6
http://purl.uniprot.org/uniprot/Q8IU82http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/1844B0E12E637B0C94FC9A1365B54EEC40853D112C1DD3E3B305146A0CE420C57B2F8670811B71B661451AC1EBC8D4E6
http://purl.uniprot.org/uniprot/#_Q8IU82-mappedCitation-29318406http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/1844B0E12E637B0C94FC9A1365B54EEC40853D112C1DD3E3B305146A0CE420C57B2F8670811B71B661451AC1EBC8D4E6