Results

RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/SHA-384/3771BA2AD468C3F0FB7357CD111FEA8B3ED080865CD7BD05C3A989C9E8484850ECE77F396DC4F8E3880D7DEB95455208http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/3771BA2AD468C3F0FB7357CD111FEA8B3ED080865CD7BD05C3A989C9E8484850ECE77F396DC4F8E3880D7DEB95455208http://www.w3.org/2000/01/rdf-schema#comment"The Arg144Gln mutation in OLFM2 is a possible disease-causing mutation in Japanese patients with OAG. Common polymorphisms in OLFM2 and OPTN may interactively contribute to the development of OAG indicating a polygenic etiology; Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)"xsd:string
http://purl.uniprot.org/uniprot/#_5AA3198B8FDFF335380BCD5B8B01E2E04DF50164CA2E0FEFEFB4D19065018D2382F20A5AD935AD68C5530BC2F93ED713http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/3771BA2AD468C3F0FB7357CD111FEA8B3ED080865CD7BD05C3A989C9E8484850ECE77F396DC4F8E3880D7DEB95455208
http://purl.uniprot.org/uniprot/O95897http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/3771BA2AD468C3F0FB7357CD111FEA8B3ED080865CD7BD05C3A989C9E8484850ECE77F396DC4F8E3880D7DEB95455208
http://purl.uniprot.org/uniprot/#_O95897-mappedCitation-17122126http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/3771BA2AD468C3F0FB7357CD111FEA8B3ED080865CD7BD05C3A989C9E8484850ECE77F396DC4F8E3880D7DEB95455208