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DESCRIBE <http://purl.uniprot.org/SHA-384/482608A7F8C4DFE9041DCBC5BB84AE6D8346B3DE70DE18C335B7B775C7E7DD4F447075C88FF544B02978EBF84A702C21>
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http://purl.uniprot.org/SHA-384/482608A7F8C4DFE9041DCBC5BB84AE6D8346B3DE70DE18C335B7B775C7E7DD4F447075C88FF544B02978EBF84A702C21
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/482608A7F8C4DFE9041DCBC5BB84AE6D8346B3DE70DE18C335B7B775C7E7DD4F447075C88FF544B02978EBF84A702C21
http://www.w3.org/2000/01/rdf-schema#comment
"This is the fourth report detailing homozygous FOXE3 mutations causing anterior segment abnormalities in human patients."
xsd:string
http://purl.uniprot.org/uniprot/#_39860EC997C9C9795B701B54A29C1DF4829F1A9F0D30A879CD403DF52E71E8BAE801D7B1EF833388100B278053EB79FF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/482608A7F8C4DFE9041DCBC5BB84AE6D8346B3DE70DE18C335B7B775C7E7DD4F447075C88FF544B02978EBF84A702C21
http://purl.uniprot.org/uniprot/A0A0A1EII5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/482608A7F8C4DFE9041DCBC5BB84AE6D8346B3DE70DE18C335B7B775C7E7DD4F447075C88FF544B02978EBF84A702C21
http://purl.uniprot.org/uniprot/#_A0A0A1EII5-mappedCitation-20664696
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/482608A7F8C4DFE9041DCBC5BB84AE6D8346B3DE70DE18C335B7B775C7E7DD4F447075C88FF544B02978EBF84A702C21