PubMed:19048115 / 493-647 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T4","span":{"begin":0,"end":154},"obj":"Sentence"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-entities","denotations":[{"id":"5565","span":{"begin":72,"end":76},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5566","span":{"begin":96,"end":102},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5567","span":{"begin":145,"end":148},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A15","pred":"db_id","subj":"5565","obj":"MESH:D010051"},{"id":"A16","pred":"db_id","subj":"5566","obj":"MESH:D009369"},{"id":"A17","pred":"db_id","subj":"5567","obj":"NCBIGene:4763"}],"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":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T19","span":{"begin":58,"end":63},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":72,"end":76},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":96,"end":102},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":145,"end":148},"obj":"GeneOrGeneProduct"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T13","span":{"begin":145,"end":148},"obj":"GeneOrGeneProduct"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T6","span":{"begin":96,"end":102},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A6","pred":"originalLabel","subj":"T6","obj":"D009369"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T9","span":{"begin":145,"end":148},"obj":"GeneOrGeneProduct"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T8","span":{"begin":145,"end":148},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"mondo_id","subj":"T8","obj":"0018975"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T8","span":{"begin":72,"end":76},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":96,"end":102},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"ID:","subj":"T8","obj":"DISEASE"},{"id":"A9","pred":"ID:","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"ID:","subj":"T9","obj":"D009369"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T8","span":{"begin":72,"end":76},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":96,"end":102},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"#label","subj":"T8","obj":"DISEASE"},{"id":"A9","pred":"#label","subj":"T9","obj":"D009369"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T9","span":{"begin":145,"end":148},"obj":"GeneOrGeneProduct"},{"id":"T86660","span":{"begin":96,"end":102},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T20393","span":{"begin":72,"end":76},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"#label","subj":"T86660","obj":"D009369"},{"id":"A8","pred":"#label","subj":"T20393","obj":"DISEASE"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}

{"project":"PMID_GLOBAL","denotations":[{"id":"T8","span":{"begin":145,"end":148},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"mondo_id","subj":"T8","obj":"0018975"}],"text":"Using a genome-wide screen of DNA copy number alterations in 36 primary OSCs, we identified two tumors with apparent homozygous deletions of the NF1 gene."}