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DESCRIBE <http://purl.uniprot.org/SHA-384/7B5949A3289EDE0990A69AF6517C4AE3F08B7738D895F43BC24F762D5557E5BD43EDDD041A03C90389ECB568E3BC7EF9>
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http://purl.uniprot.org/SHA-384/7B5949A3289EDE0990A69AF6517C4AE3F08B7738D895F43BC24F762D5557E5BD43EDDD041A03C90389ECB568E3BC7EF9
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7B5949A3289EDE0990A69AF6517C4AE3F08B7738D895F43BC24F762D5557E5BD43EDDD041A03C90389ECB568E3BC7EF9
http://www.w3.org/2000/01/rdf-schema#comment
"The presence of a hypointense pituitary lesion and other clinical findings broadens the phenotype associated with LHX3 gene mutation."
xsd:string
http://purl.uniprot.org/uniprot/#_9B7B7F96FD8253C295DCD67F51D9B9A7AFE900AB48ADD1F6A59D810BE437057A1007BA4170A41699A47BDF4AA998780E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7B5949A3289EDE0990A69AF6517C4AE3F08B7738D895F43BC24F762D5557E5BD43EDDD041A03C90389ECB568E3BC7EF9
http://purl.uniprot.org/uniprot/F1T0D5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7B5949A3289EDE0990A69AF6517C4AE3F08B7738D895F43BC24F762D5557E5BD43EDDD041A03C90389ECB568E3BC7EF9
http://purl.uniprot.org/uniprot/#_F1T0D5-mappedCitation-16394081
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7B5949A3289EDE0990A69AF6517C4AE3F08B7738D895F43BC24F762D5557E5BD43EDDD041A03C90389ECB568E3BC7EF9