PubMed:15754732 / 0-164 JSONTXT

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    LitCoin-sentences

    {"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":122},"obj":"Sentence"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin-entities

    {"project":"LitCoin-entities","denotations":[{"id":"1545","span":{"begin":14,"end":18},"obj":"GeneOrGeneProduct"},{"id":"1546","span":{"begin":48,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"1547","span":{"begin":123,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"1548","span":{"begin":152,"end":156},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"db_id","subj":"1545","obj":"NCBIGene:4221"},{"id":"A2","pred":"db_id","subj":"1546","obj":"MESH:D049950"},{"id":"A3","pred":"db_id","subj":"1547","obj":"MESH:D049950"},{"id":"A4","pred":"db_id","subj":"1548","obj":"MESH:D049950"}],"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":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin_Mondo

    {"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":48,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":56,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":123,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":131,"end":150},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0010837"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0001741"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0010837"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0001741"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin-GeneOrGeneProduct-v0

    {"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":0,"end":5},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":14,"end":18},"obj":"GeneOrGeneProduct"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin-GeneOrGeneProduct-v2

    {"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":0,"end":5},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":14,"end":18},"obj":"GeneOrGeneProduct"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin-Disease-MeSH

    {"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":48,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":123,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":152,"end":156},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D049950"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D049950"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"D049950"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin_Mondo_095

    {"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":14,"end":18},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":48,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":123,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":152,"end":156},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0007540"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0010837"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0010837"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0010837"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin-MeSH-Disease-2

    {"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":14,"end":18},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":48,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":123,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":152,"end":156},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"DISEASE"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D049950"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D049950"},{"id":"A4","pred":"ID:","subj":"T4","obj":"D049950"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin-MONDO_bioort2019

    {"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":48,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":123,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":152,"end":156},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D049950"},{"id":"A2","pred":"#label","subj":"T2","obj":"D049950"},{"id":"A3","pred":"#label","subj":"T3","obj":"D049950"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    LitCoin-training-merged

    {"project":"LitCoin-training-merged","denotations":[{"id":"T95728","span":{"begin":152,"end":156},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":123,"end":150},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T38477","span":{"begin":48,"end":75},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A77742","pred":"#label","subj":"T95728","obj":"D049950"},{"id":"A39529","pred":"#label","subj":"T2","obj":"D049950"},{"id":"A19849","pred":"#label","subj":"T38477","obj":"D049950"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"15754732-0#14#18#gene4221","span":{"begin":14,"end":18},"obj":"gene4221"},{"id":"15754732-0#48#75#diseaseC0221002","span":{"begin":48,"end":75},"obj":"diseaseC0221002"}],"relations":[{"id":"14#18#gene422148#75#diseaseC0221002","pred":"associated_with","subj":"15754732-0#14#18#gene4221","obj":"15754732-0#48#75#diseaseC0221002"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}

    DisGeNET

    {"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":14,"end":18},"obj":"gene:4221"},{"id":"T1","span":{"begin":48,"end":75},"obj":"disease:C0221002"},{"id":"T3","span":{"begin":152,"end":156},"obj":"disease:C0221002"},{"id":"T5","span":{"begin":123,"end":150},"obj":"disease:C0221002"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.\nPrimary hyperparathyroidism (pHPT) is a c"}