PubMed:15951966 / 0-196 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":68},"obj":"Sentence"},{"id":"T2","span":{"begin":69,"end":80},"obj":"Sentence"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-entities","denotations":[{"id":"1944","span":{"begin":46,"end":50},"obj":"GeneOrGeneProduct"},{"id":"1945","span":{"begin":55,"end":59},"obj":"GeneOrGeneProduct"},{"id":"1946","span":{"begin":101,"end":105},"obj":"GeneOrGeneProduct"},{"id":"1947","span":{"begin":110,"end":114},"obj":"GeneOrGeneProduct"},{"id":"1948","span":{"begin":172,"end":177},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"db_id","subj":"1944","obj":"NCBIGene:4436"},{"id":"A2","pred":"db_id","subj":"1945","obj":"NCBIGene:4292"},{"id":"A3","pred":"db_id","subj":"1946","obj":"NCBIGene:4436"},{"id":"A4","pred":"db_id","subj":"1947","obj":"NCBIGene:4292"},{"id":"A5","pred":"db_id","subj":"1948","obj":"MESH:D003123"}],"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":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-SeqVar","denotations":[{"id":"T1","span":{"begin":57,"end":64},"obj":"SequenceVariant"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":33,"end":42},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":46,"end":50},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":55,"end":59},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":101,"end":105},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":110,"end":114},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":151,"end":159},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":172,"end":177},"obj":"GeneOrGeneProduct"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":46,"end":50},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":55,"end":59},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":101,"end":105},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":110,"end":114},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":172,"end":177},"obj":"GeneOrGeneProduct"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":172,"end":177},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"DISEASE"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":46,"end":50},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":55,"end":59},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":101,"end":105},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":110,"end":114},"obj":"GeneOrGeneProduct"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":172,"end":177},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0018630"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":172,"end":177},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"DISEASE"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":172,"end":177},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"DISEASE"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}

{"project":"LitCoin-training-merged","denotations":[{"id":"T4","span":{"begin":110,"end":114},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":101,"end":105},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":55,"end":59},"obj":"GeneOrGeneProduct"},{"id":"T1","span":{"begin":46,"end":50},"obj":"GeneOrGeneProduct"},{"id":"T45079","span":{"begin":172,"end":177},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T96994","span":{"begin":57,"end":64},"obj":"SequenceVariant"}],"attributes":[{"id":"A1","pred":"#label","subj":"T45079","obj":"DISEASE"}],"text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous "}