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DESCRIBE <http://purl.uniprot.org/SHA-384/AECA1EBE0576B5CC1006227E5015E5DA399639CA609EF244859970BEE81CD532121E02904CAE467F647D6A6284DF2A58>
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http://purl.uniprot.org/SHA-384/AECA1EBE0576B5CC1006227E5015E5DA399639CA609EF244859970BEE81CD532121E02904CAE467F647D6A6284DF2A58
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/AECA1EBE0576B5CC1006227E5015E5DA399639CA609EF244859970BEE81CD532121E02904CAE467F647D6A6284DF2A58
http://www.w3.org/2000/01/rdf-schema#comment
"These results reveal that mutations in TFAP2A are associated with a wide range of eye phenotypes and that hypomorphic tfap2a mutations can increase the risk of developmental defects arising from mutations at other loci."
xsd:string
http://purl.uniprot.org/uniprot/#_E59A07B6ECF7A1D2BEB314CB9843F84E991F3A0C1CCAD7216B91457CCD6ABA3BECEC7765B5EF746EF640177EAB834681
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/AECA1EBE0576B5CC1006227E5015E5DA399639CA609EF244859970BEE81CD532121E02904CAE467F647D6A6284DF2A58
http://purl.uniprot.org/uniprot/F1QUT4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AECA1EBE0576B5CC1006227E5015E5DA399639CA609EF244859970BEE81CD532121E02904CAE467F647D6A6284DF2A58
http://purl.uniprot.org/uniprot/#_F1QUT4-mappedCitation-19685247
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AECA1EBE0576B5CC1006227E5015E5DA399639CA609EF244859970BEE81CD532121E02904CAE467F647D6A6284DF2A58