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DESCRIBE <http://purl.uniprot.org/SHA-384/782FCBA998D89EE3D5009F0E89B2A1BAE4945CB582E25385F7E39567474B32B82A2126F9698FCF9C6657BA1641F6AB56>
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http://purl.uniprot.org/SHA-384/782FCBA998D89EE3D5009F0E89B2A1BAE4945CB582E25385F7E39567474B32B82A2126F9698FCF9C6657BA1641F6AB56
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/782FCBA998D89EE3D5009F0E89B2A1BAE4945CB582E25385F7E39567474B32B82A2126F9698FCF9C6657BA1641F6AB56
http://www.w3.org/2000/01/rdf-schema#comment
"Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia."
xsd:string
http://purl.uniprot.org/uniprot/#_C3A0C2B88582A7083C3AB5FFAA042EFAC7C947718E227C43F681A6F24A907D406DD167DC48FF1C753A25CBA59ABDE352
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/782FCBA998D89EE3D5009F0E89B2A1BAE4945CB582E25385F7E39567474B32B82A2126F9698FCF9C6657BA1641F6AB56
http://purl.uniprot.org/uniprot/A0A0A1EII5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/782FCBA998D89EE3D5009F0E89B2A1BAE4945CB582E25385F7E39567474B32B82A2126F9698FCF9C6657BA1641F6AB56
http://purl.uniprot.org/uniprot/#_A0A0A1EII5-mappedCitation-37758467
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/782FCBA998D89EE3D5009F0E89B2A1BAE4945CB582E25385F7E39567474B32B82A2126F9698FCF9C6657BA1641F6AB56