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Q34404974-1A935F5E-5DA3-49B9-9666-94A278A61DDD
Q34404974-1A935F5E-5DA3-49B9-9666-94A278A61DDD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34404974-1A935F5E-5DA3-49B9-9666-94A278A61DDD
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.
P2860
Q34404974-1A935F5E-5DA3-49B9-9666-94A278A61DDD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34404974-1A935F5E-5DA3-49B9-9666-94A278A61DDD
rank
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type
BestRank
Statement
wasDerivedFrom
6a5b8032d764c58c123aae0d85b1ca89a9b5da1b
P2860
Novel TULP1 mutation causing leber congenital amaurosis or early onset retinal degeneration.