PubMed:16200390 / 751-1031 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T5","span":{"begin":0,"end":280},"obj":"Sentence"}],"text":"This objective was undertaken using a high-throughput DNA pooling experimental design, which proved to be a very accurate, sensitive and specific method of estimating allele frequencies for single nucleotide polymorphism, insertion deletion and variable number tandem repeat loci."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T20","span":{"begin":38,"end":42},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":146,"end":152},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":174,"end":185},"obj":"GeneOrGeneProduct"}],"text":"This objective was undertaken using a high-throughput DNA pooling experimental design, which proved to be a very accurate, sensitive and specific method of estimating allele frequencies for single nucleotide polymorphism, insertion deletion and variable number tandem repeat loci."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T15","span":{"begin":38,"end":42},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":146,"end":152},"obj":"GeneOrGeneProduct"}],"text":"This objective was undertaken using a high-throughput DNA pooling experimental design, which proved to be a very accurate, sensitive and specific method of estimating allele frequencies for single nucleotide polymorphism, insertion deletion and variable number tandem repeat loci."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T9","span":{"begin":123,"end":132},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"mondo_id","subj":"T9","obj":"0000605"}],"text":"This objective was undertaken using a high-throughput DNA pooling experimental design, which proved to be a very accurate, sensitive and specific method of estimating allele frequencies for single nucleotide polymorphism, insertion deletion and variable number tandem repeat loci."}