PubMed:15033202 / 355-515 JSONTXT

{"project":"LitCoin-entities","denotations":[{"id":"582","span":{"begin":5,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"583","span":{"begin":32,"end":40},"obj":"OrganismTaxon"},{"id":"584","span":{"begin":121,"end":142},"obj":"SequenceVariant"},{"id":"585","span":{"begin":150,"end":154},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A9","pred":"db_id","subj":"582","obj":"MESH:D049932"},{"id":"A10","pred":"db_id","subj":"583","obj":"NCBITaxon:9606"},{"id":"A11","pred":"db_id","subj":"584","obj":"c|DEL||5"},{"id":"A12","pred":"db_id","subj":"585","obj":"NCBIGene:4683"}],"namespaces":[{"prefix":"_base","uri":"https://w3id.org/biolink/vocab/"},{"prefix":"MESH","uri":"http://id.nlm.nih.gov/mesh/"},{"prefix":"NCBITaxon","uri":"https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id="},{"prefix":"NCBIGene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"OMIM","uri":"https://www.omim.org/entry/"},{"prefix":"DBSNP","uri":"https://www.ncbi.nlm.nih.gov/snp/"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-sentences","denotations":[{"id":"T3","span":{"begin":0,"end":160},"obj":"Sentence"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T7","span":{"begin":5,"end":31},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"mondo_id","subj":"T7","obj":"0009623"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T8","span":{"begin":23,"end":31},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":69,"end":72},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":76,"end":80},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":150,"end":154},"obj":"GeneOrGeneProduct"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T8","span":{"begin":23,"end":31},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":150,"end":154},"obj":"GeneOrGeneProduct"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T7","span":{"begin":5,"end":31},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"originalLabel","subj":"T7","obj":"D049932"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T3","span":{"begin":5,"end":31},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":150,"end":154},"obj":"GeneOrGeneProduct"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T6","span":{"begin":5,"end":31},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0009623"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T9","span":{"begin":5,"end":31},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"ID:","subj":"T9","obj":"D049932"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T9","span":{"begin":5,"end":31},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"#label","subj":"T9","obj":"D049932"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":32,"end":40},"obj":"OrganismTaxon"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T4","span":{"begin":150,"end":154},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":5,"end":31},"obj":"GeneOrGeneProduct"},{"id":"T66189","span":{"begin":5,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T96819","span":{"begin":32,"end":40},"obj":"OrganismTaxon"}],"attributes":[{"id":"A9","pred":"#label","subj":"T66189","obj":"D049932"}],"text":"Most Nijmegen breakage syndrome patients are of Slavonic origin, and all of them known so far carry a founder homozygous 5 nucleotide deletion in the NBS1 gene."}