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http://purl.uniprot.org/SHA-384/136970BC3CC20D0ABB1BBE50FDE21600AEC5280AA7D375C613DF32F491DF62E8BFA4F535D75972942A8C8BF80DBC5159http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/136970BC3CC20D0ABB1BBE50FDE21600AEC5280AA7D375C613DF32F491DF62E8BFA4F535D75972942A8C8BF80DBC5159http://www.w3.org/2000/01/rdf-schema#comment"Blockade of MER proto-oncogene tyrosine kinase (MerTK) results in accumulation of apoptotic cells within tumors and triggers type I interferon response. Treatment of tumor-bearing mice with anti-MerTK antibody stimulates T cell activation and synergizes with anti-PD-1 or anti-PD-L1 therapy. Abolishing cGAMP production depleting extracellular ATP or inactivating ATP-gated P2X7R channel compromises anti-MerTK blockade."xsd:string
http://purl.uniprot.org/uniprot/#_907DD403BF14FAB8CDB33F827D83FA2237D8AC9A01742247F03BD79D3D09857345758D73A1596C0C029ECE706AF5F139http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/136970BC3CC20D0ABB1BBE50FDE21600AEC5280AA7D375C613DF32F491DF62E8BFA4F535D75972942A8C8BF80DBC5159
http://purl.uniprot.org/uniprot/Q60805http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/136970BC3CC20D0ABB1BBE50FDE21600AEC5280AA7D375C613DF32F491DF62E8BFA4F535D75972942A8C8BF80DBC5159
http://purl.uniprot.org/uniprot/#_Q60805-mappedCitation-32049051http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/136970BC3CC20D0ABB1BBE50FDE21600AEC5280AA7D375C613DF32F491DF62E8BFA4F535D75972942A8C8BF80DBC5159