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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/E110464670DC2215B952E7466B0EB17D921C39E3EFF20A27E01F081B1EDA4F35207E874325759E03E47DC664C48D8FF2>
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http://purl.uniprot.org/SHA-384/E110464670DC2215B952E7466B0EB17D921C39E3EFF20A27E01F081B1EDA4F35207E874325759E03E47DC664C48D8FF2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E110464670DC2215B952E7466B0EB17D921C39E3EFF20A27E01F081B1EDA4F35207E874325759E03E47DC664C48D8FF2
http://www.w3.org/2000/01/rdf-schema#comment
"The TULP1 allele p.Gln301* represents a founder mutation on the Arabian Peninsula and is associated with a recognisable congenital recessive rod-cone dystrophy phenotype in the homozygous state."
xsd:string
http://purl.uniprot.org/uniprot/#_C112FB2757A7E1C9B2C4E9C8B4D882131AF322530A291AA2426533F80AB0704F8713CEC3444B68B630FCB8AF4436813F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E110464670DC2215B952E7466B0EB17D921C39E3EFF20A27E01F081B1EDA4F35207E874325759E03E47DC664C48D8FF2
http://purl.uniprot.org/uniprot/Q0QD38
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E110464670DC2215B952E7466B0EB17D921C39E3EFF20A27E01F081B1EDA4F35207E874325759E03E47DC664C48D8FF2
http://purl.uniprot.org/uniprot/#_Q0QD38-mappedCitation-25342276
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E110464670DC2215B952E7466B0EB17D921C39E3EFF20A27E01F081B1EDA4F35207E874325759E03E47DC664C48D8FF2