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DESCRIBE <http://purl.uniprot.org/SHA-384/4531D96243A578726E4B657E3F436C3608835B5CEEBC2997437B8E7143ABACE4AECE4B15D33C74C1EBC9ADE8C1839F58>
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http://purl.uniprot.org/SHA-384/4531D96243A578726E4B657E3F436C3608835B5CEEBC2997437B8E7143ABACE4AECE4B15D33C74C1EBC9ADE8C1839F58
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4531D96243A578726E4B657E3F436C3608835B5CEEBC2997437B8E7143ABACE4AECE4B15D33C74C1EBC9ADE8C1839F58
http://www.w3.org/2000/01/rdf-schema#comment
"Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia."
xsd:string
http://purl.uniprot.org/uniprot/#_B2DA293AD677BE77D25F75DB0830F2EFBA5366985C10F7B88919DD3BF032B9802FAAF9BE400711CD87769D37F6A8D6AA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4531D96243A578726E4B657E3F436C3608835B5CEEBC2997437B8E7143ABACE4AECE4B15D33C74C1EBC9ADE8C1839F58
http://purl.uniprot.org/uniprot/B4DGR6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4531D96243A578726E4B657E3F436C3608835B5CEEBC2997437B8E7143ABACE4AECE4B15D33C74C1EBC9ADE8C1839F58
http://purl.uniprot.org/uniprot/#_B4DGR6-mappedCitation-33517396
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4531D96243A578726E4B657E3F436C3608835B5CEEBC2997437B8E7143ABACE4AECE4B15D33C74C1EBC9ADE8C1839F58