PubMed:17166870 / 0-207 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":113},"obj":"Sentence"},{"id":"T2","span":{"begin":114,"end":125},"obj":"Sentence"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin-entities","denotations":[{"id":"3693","span":{"begin":23,"end":31},"obj":"GeneOrGeneProduct"},{"id":"3694","span":{"begin":54,"end":72},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3695","span":{"begin":81,"end":112},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3696","span":{"begin":126,"end":144},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3697","span":{"begin":146,"end":149},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"db_id","subj":"3693","obj":"NCBIGene:2022"},{"id":"A2","pred":"db_id","subj":"3694","obj":"MESH:D012595"},{"id":"A3","pred":"db_id","subj":"3695","obj":"MESH:D000081029"},{"id":"A4","pred":"db_id","subj":"3696","obj":"MESH:D012595"},{"id":"A5","pred":"db_id","subj":"3697","obj":"MESH:D012595"}],"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":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":54,"end":72},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":81,"end":112},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":126,"end":144},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0005100"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0015924"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0005100"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":23,"end":31},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":100,"end":112},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":200,"end":205},"obj":"GeneOrGeneProduct"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

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{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":54,"end":72},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":81,"end":112},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":126,"end":144},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":146,"end":149},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D012595"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D000081029"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"D012595"},{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D012595"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":23,"end":31},"obj":"GeneOrGeneProduct"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":54,"end":72},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":81,"end":112},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":126,"end":144},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":146,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":156,"end":182},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0005100"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0024533"},{"id":"A3","pred":"mondo_id","subj":"T2","obj":"0015924"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0005100"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0005100"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0003900"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":54,"end":72},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":81,"end":112},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":126,"end":144},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":146,"end":149},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D012595"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D000081029"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D012595"},{"id":"A4","pred":"ID:","subj":"T4","obj":"D012595"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":54,"end":72},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":81,"end":112},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":126,"end":144},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":146,"end":149},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D012595"},{"id":"A2","pred":"#label","subj":"T2","obj":"D000081029"},{"id":"A3","pred":"#label","subj":"T3","obj":"D012595"},{"id":"A4","pred":"#label","subj":"T4","obj":"D012595"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"LitCoin-training-merged","denotations":[{"id":"T3851","span":{"begin":23,"end":31},"obj":"GeneOrGeneProduct"},{"id":"T65914","span":{"begin":146,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T88367","span":{"begin":126,"end":144},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T96334","span":{"begin":81,"end":112},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T94954","span":{"begin":54,"end":72},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A33062","pred":"#label","subj":"T65914","obj":"D012595"},{"id":"A45498","pred":"#label","subj":"T88367","obj":"D012595"},{"id":"A70216","pred":"#label","subj":"T96334","obj":"D000081029"},{"id":"A29051","pred":"#label","subj":"T94954","obj":"D012595"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":23,"end":31},"obj":"gene:2022"},{"id":"T1","span":{"begin":54,"end":72},"obj":"disease:C0036421"},{"id":"T2","span":{"begin":23,"end":31},"obj":"gene:2022"},{"id":"T3","span":{"begin":81,"end":112},"obj":"disease:C0152171"},{"id":"T4","span":{"begin":23,"end":31},"obj":"gene:2022"},{"id":"T5","span":{"begin":81,"end":112},"obj":"disease:C2973725"},{"id":"T6","span":{"begin":23,"end":31},"obj":"gene:2022"},{"id":"T7","span":{"begin":81,"end":112},"obj":"disease:C3714844"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"},{"id":"R3","pred":"associated_with","subj":"T4","obj":"T5"},{"id":"R4","pred":"associated_with","subj":"T6","obj":"T7"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":156,"end":182},"obj":"HP_0003549"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"17166870-0#23#31#gene2022","span":{"begin":23,"end":31},"obj":"gene2022"},{"id":"17166870-0#54#72#diseaseC0036421","span":{"begin":54,"end":72},"obj":"diseaseC0036421"},{"id":"17166870-0#81#112#diseaseC3203102","span":{"begin":81,"end":112},"obj":"diseaseC3203102"}],"relations":[{"id":"23#31#gene202254#72#diseaseC0036421","pred":"associated_with","subj":"17166870-0#23#31#gene2022","obj":"17166870-0#54#72#diseaseC0036421"},{"id":"23#31#gene202281#112#diseaseC3203102","pred":"associated_with","subj":"17166870-0#23#31#gene2022","obj":"17166870-0#81#112#diseaseC3203102"}],"text":"Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.\nUNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by early g"}