RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/SHA-384/6D3779A1AE9C5C859C6B78F3EF617C2FA5CECFE380461CA99E2DE6705DC448D22BD7BF62825D1D766FD3D6F76EF99FD5http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6D3779A1AE9C5C859C6B78F3EF617C2FA5CECFE380461CA99E2DE6705DC448D22BD7BF62825D1D766FD3D6F76EF99FD5http://www.w3.org/2000/01/rdf-schema#comment"Heterozygous pathogenic variants in the PITX2 and FOXC1 genes accounted for 66% (6/9) of the ARS/ASD cases. The absence of PAX6 or CYP1B1 abnormalities could reflect our small sample size although their analysis could be justified in ARS/ASD patients that present with congenital glaucoma or aniridia."xsd:string
http://purl.uniprot.org/uniprot/#_08448803147B816BB20FD4C42FF1F3348F7539B8834108F34B541EB7D3A582F2CBD6A4033233E6FB535443F2EB5BA552http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/6D3779A1AE9C5C859C6B78F3EF617C2FA5CECFE380461CA99E2DE6705DC448D22BD7BF62825D1D766FD3D6F76EF99FD5
http://purl.uniprot.org/uniprot/A0A1W2PRA8http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/6D3779A1AE9C5C859C6B78F3EF617C2FA5CECFE380461CA99E2DE6705DC448D22BD7BF62825D1D766FD3D6F76EF99FD5
http://purl.uniprot.org/uniprot/#_A0A1W2PRA8-mappedCitation-30457409http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/6D3779A1AE9C5C859C6B78F3EF617C2FA5CECFE380461CA99E2DE6705DC448D22BD7BF62825D1D766FD3D6F76EF99FD5