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DESCRIBE <http://purl.uniprot.org/SHA-384/D43AA5260FE40A3811AEF847142F33F4FF673556A2F71257C6F36FFA01AA38619DA81B1E4DD7ECF0183A88319DA0F5D5>
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http://purl.uniprot.org/SHA-384/D43AA5260FE40A3811AEF847142F33F4FF673556A2F71257C6F36FFA01AA38619DA81B1E4DD7ECF0183A88319DA0F5D5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D43AA5260FE40A3811AEF847142F33F4FF673556A2F71257C6F36FFA01AA38619DA81B1E4DD7ECF0183A88319DA0F5D5
http://www.w3.org/2000/01/rdf-schema#comment
"A homozygous deletion was identified in the NPHP1 gene spanning at least from exon 5 to exon 20 in two families in Iranian children with nephronophthisis."
xsd:string
http://purl.uniprot.org/uniprot/#_50C007E7A38A6A1871F4C064798EEBE30DE00888186831411BC30E343A283BD27C8927095582F3BAFE3E9F01F4B98254
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D43AA5260FE40A3811AEF847142F33F4FF673556A2F71257C6F36FFA01AA38619DA81B1E4DD7ECF0183A88319DA0F5D5
http://purl.uniprot.org/uniprot/C9J082
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D43AA5260FE40A3811AEF847142F33F4FF673556A2F71257C6F36FFA01AA38619DA81B1E4DD7ECF0183A88319DA0F5D5
http://purl.uniprot.org/uniprot/#_C9J082-mappedCitation-25851290
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D43AA5260FE40A3811AEF847142F33F4FF673556A2F71257C6F36FFA01AA38619DA81B1E4DD7ECF0183A88319DA0F5D5