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Q41696457-0D099B11-996E-4B15-9066-F725C155B72E
Q41696457-0D099B11-996E-4B15-9066-F725C155B72E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41696457-0D099B11-996E-4B15-9066-F725C155B72E
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome.
P2860
Q41696457-0D099B11-996E-4B15-9066-F725C155B72E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41696457-0D099B11-996E-4B15-9066-F725C155B72E
rank
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Statement
wasDerivedFrom
a196980d05ee2eebcdcf7afac26fa6a8582fd28d
P2860
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation