PubMed:18366737 / 453-625 JSONTXT

{"project":"PMID_GLOBAL","denotations":[{"id":"T8","span":{"begin":22,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":89,"end":91},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":109,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":153,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"mondo_id","subj":"T8","obj":"0001572"},{"id":"A9","pred":"mondo_id","subj":"T9","obj":"0016525"},{"id":"A10","pred":"mondo_id","subj":"T10","obj":"0007888"},{"id":"A11","pred":"mondo_id","subj":"T11","obj":"0007888"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-sentences","denotations":[{"id":"T5","span":{"begin":0,"end":172},"obj":"Sentence"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

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{"project":"LitCoin_Mondo","denotations":[{"id":"T2","span":{"begin":22,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":140,"end":150},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0001572"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0001572"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T12","span":{"begin":13,"end":21},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":109,"end":117},"obj":"GeneOrGeneProduct"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T17","span":{"begin":13,"end":21},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":76,"end":85},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":109,"end":117},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":153,"end":157},"obj":"GeneOrGeneProduct"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T5","span":{"begin":22,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":140,"end":150},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"originalLabel","subj":"T5","obj":"D007889"},{"id":"A6","pred":"originalLabel","subj":"T6","obj":"D007889"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T8","span":{"begin":22,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":89,"end":91},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":109,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":153,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"mondo_id","subj":"T8","obj":"0001572"},{"id":"A9","pred":"mondo_id","subj":"T9","obj":"0016525"},{"id":"A10","pred":"mondo_id","subj":"T10","obj":"0007888"},{"id":"A11","pred":"mondo_id","subj":"T11","obj":"0007888"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T8","span":{"begin":22,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":109,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":153,"end":157},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":159,"end":170},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"ID:","subj":"T8","obj":"D007889"},{"id":"A9","pred":"ID:","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"ID:","subj":"T10","obj":"DISEASE"},{"id":"A11","pred":"ID:","subj":"T11","obj":"DISEASE"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T7","span":{"begin":22,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":109,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":153,"end":157},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":159,"end":170},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"#label","subj":"T7","obj":"D007889"},{"id":"A8","pred":"#label","subj":"T8","obj":"DISEASE"},{"id":"A9","pred":"#label","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"#label","subj":"T10","obj":"DISEASE"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":95,"end":103},"obj":"OrganismTaxon"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T30897","span":{"begin":159,"end":170},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T77092","span":{"begin":153,"end":157},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T43739","span":{"begin":109,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T50201","span":{"begin":22,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T73931","span":{"begin":95,"end":103},"obj":"OrganismTaxon"}],"attributes":[{"id":"A18707","pred":"#label","subj":"T30897","obj":"DISEASE"},{"id":"A47809","pred":"#label","subj":"T77092","obj":"DISEASE"},{"id":"A36893","pred":"#label","subj":"T43739","obj":"DISEASE"},{"id":"A96163","pred":"#label","subj":"T50201","obj":"D007889"}],"text":"In 2002, the Multiple Leiomyoma Consortium identified heterozygous germline mutations of FH in patients with multiple cutaneous and uterine leiomyomas, (MCUL: OMIM 150800)."}