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DESCRIBE <http://purl.uniprot.org/SHA-384/2EC1D7F9FA00898FE128A3AB15575FABF735384E6860DD9B7C772F90F9437DF6939096510FA419BDA47A0AACB9A76724>
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http://purl.uniprot.org/SHA-384/2EC1D7F9FA00898FE128A3AB15575FABF735384E6860DD9B7C772F90F9437DF6939096510FA419BDA47A0AACB9A76724
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2EC1D7F9FA00898FE128A3AB15575FABF735384E6860DD9B7C772F90F9437DF6939096510FA419BDA47A0AACB9A76724
http://www.w3.org/2000/01/rdf-schema#comment
"These results demonstrate that in C57BL/6Jmice Fscn2 is essential for maintaining ear and eye function and that a null mutation of Fscn2 leads to progressive hearing loss and retinal degeneration."
xsd:string
http://purl.uniprot.org/uniprot/#_0DACA928E569EE86463B95C28B94AA833B4079A8E454116456FFEA8DF85E24F618141813D196CFC5453214F5C94668FB
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/2EC1D7F9FA00898FE128A3AB15575FABF735384E6860DD9B7C772F90F9437DF6939096510FA419BDA47A0AACB9A76724
http://purl.uniprot.org/uniprot/Q32M02
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2EC1D7F9FA00898FE128A3AB15575FABF735384E6860DD9B7C772F90F9437DF6939096510FA419BDA47A0AACB9A76724
http://purl.uniprot.org/uniprot/#_Q32M02-mappedCitation-30082328
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2EC1D7F9FA00898FE128A3AB15575FABF735384E6860DD9B7C772F90F9437DF6939096510FA419BDA47A0AACB9A76724