Results

RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/SHA-384/A6539079699B46B3F4F080B89ED1C89589903D2FE71B959349384C10C32D8B0F6BDBE709B82A671B4CFEBD9DFF67087Dhttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A6539079699B46B3F4F080B89ED1C89589903D2FE71B959349384C10C32D8B0F6BDBE709B82A671B4CFEBD9DFF67087Dhttp://www.w3.org/2000/01/rdf-schema#comment"A questionnaire based study provides evidence that the hereditary hemorrhagic telangietasia (HHT) phenotype caused by mutations in endoglin (HHT1) is distinct from and more severe than HHT caused by mutations in ALK1 (HHT2); Observational study of gene-disease association. (HuGE Navigator)"xsd:string
http://purl.uniprot.org/uniprot/#_7B74F1CC7EB3CEA3BD69C4328B424ECD68B3E1B6E02A23F7B33611E8238F00C3C0E38A7BBFEAF6D0F75684FCCB0B0F9Bhttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/A6539079699B46B3F4F080B89ED1C89589903D2FE71B959349384C10C32D8B0F6BDBE709B82A671B4CFEBD9DFF67087D
http://purl.uniprot.org/uniprot/Q71V36http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/A6539079699B46B3F4F080B89ED1C89589903D2FE71B959349384C10C32D8B0F6BDBE709B82A671B4CFEBD9DFF67087D
http://purl.uniprot.org/uniprot/#_Q71V36-mappedCitation-12920067http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/A6539079699B46B3F4F080B89ED1C89589903D2FE71B959349384C10C32D8B0F6BDBE709B82A671B4CFEBD9DFF67087D