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DESCRIBE <http://purl.uniprot.org/SHA-384/82FAB75689801D08CFA820F208DDB81B56D2989D154E125FC0BE53FF0A3943DC49AD46FAA4D9ABF6BF5A06CE6F079081>
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http://purl.uniprot.org/SHA-384/82FAB75689801D08CFA820F208DDB81B56D2989D154E125FC0BE53FF0A3943DC49AD46FAA4D9ABF6BF5A06CE6F079081
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/82FAB75689801D08CFA820F208DDB81B56D2989D154E125FC0BE53FF0A3943DC49AD46FAA4D9ABF6BF5A06CE6F079081
http://www.w3.org/2000/01/rdf-schema#comment
"The results support the importance of exons near the 5' end of NRXN1 in the expression of neurodevelopmental disorders. Intronic NRXN1 deletions do not appear to substantially increase the risk for clinical phenotypes"
xsd:string
http://purl.uniprot.org/uniprot/#_7E625F1A290F7139D7DA76EAB838EE2945E324BB3C07BCC50014E323F2B6DC76C6DA47C7337C106805659EF6A8A488BD
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/82FAB75689801D08CFA820F208DDB81B56D2989D154E125FC0BE53FF0A3943DC49AD46FAA4D9ABF6BF5A06CE6F079081
http://purl.uniprot.org/uniprot/A0A0D9SEM5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/82FAB75689801D08CFA820F208DDB81B56D2989D154E125FC0BE53FF0A3943DC49AD46FAA4D9ABF6BF5A06CE6F079081
http://purl.uniprot.org/uniprot/#_A0A0D9SEM5-mappedCitation-27195815
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/82FAB75689801D08CFA820F208DDB81B56D2989D154E125FC0BE53FF0A3943DC49AD46FAA4D9ABF6BF5A06CE6F079081