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http://purl.uniprot.org/SHA-384/608863752EFA465E50EA2A2766EFACCA814A69DB0763A24053AA24566E2A987688DEEAC188A6C803E11EEB5D021652B4http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/608863752EFA465E50EA2A2766EFACCA814A69DB0763A24053AA24566E2A987688DEEAC188A6C803E11EEB5D021652B4http://www.w3.org/2000/01/rdf-schema#comment"considered alongside two recent studies of single families reporting loss of function candidate variants in CEP55 confirm disruption of CEP55 function as a cause of this clinical spectrum and enable us to delineate the cardinal clinical features of this disorder providing important new insights into early human development"xsd:string
http://purl.uniprot.org/uniprot/#_D275AB709643C4B3D44F9BF2E6917010FEDDA8C2D7863A95246784C1251B029BC50B6C078864BF52B84C2C4285583724http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/608863752EFA465E50EA2A2766EFACCA814A69DB0763A24053AA24566E2A987688DEEAC188A6C803E11EEB5D021652B4
http://purl.uniprot.org/uniprot/Q53EZ4http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/608863752EFA465E50EA2A2766EFACCA814A69DB0763A24053AA24566E2A987688DEEAC188A6C803E11EEB5D021652B4
http://purl.uniprot.org/uniprot/#_Q53EZ4-mappedCitation-30622327http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/608863752EFA465E50EA2A2766EFACCA814A69DB0763A24053AA24566E2A987688DEEAC188A6C803E11EEB5D021652B4