PubMed:20682662 / 1504-1651 JSONTXT

{"project":"Inflammaging","denotations":[{"id":"T15","span":{"begin":0,"end":147},"obj":"Sentence"},{"id":"T15","span":{"begin":0,"end":147},"obj":"Sentence"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-sentences","denotations":[{"id":"T15","span":{"begin":0,"end":147},"obj":"Sentence"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-entities","denotations":[{"id":"7783","span":{"begin":29,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7784","span":{"begin":56,"end":60},"obj":"GeneOrGeneProduct"},{"id":"7785","span":{"begin":61,"end":73},"obj":"SequenceVariant"},{"id":"7786","span":{"begin":132,"end":134},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7787","span":{"begin":136,"end":139},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7788","span":{"begin":144,"end":146},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A44","pred":"db_id","subj":"7783","obj":"MESH:D008181"},{"id":"A45","pred":"db_id","subj":"7784","obj":"NCBIGene:1234"},{"id":"A46","pred":"db_id","subj":"7785","obj":"c|DEL||32"},{"id":"A47","pred":"db_id","subj":"7786","obj":"MESH:D001172"},{"id":"A48","pred":"db_id","subj":"7787","obj":"MESH:D008180"},{"id":"A49","pred":"db_id","subj":"7788","obj":"MESH:D008181"}],"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":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T13","span":{"begin":96,"end":118},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A13","pred":"mondo_id","subj":"T13","obj":"0042489"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-SeqVar","denotations":[{"id":"T9","span":{"begin":61,"end":64},"obj":"SequenceVariant"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T21","span":{"begin":56,"end":60},"obj":"GeneOrGeneProduct"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T11","span":{"begin":56,"end":60},"obj":"GeneOrGeneProduct"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T27","span":{"begin":29,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T28","span":{"begin":96,"end":118},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T29","span":{"begin":132,"end":134},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T30","span":{"begin":136,"end":139},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T31","span":{"begin":144,"end":146},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A27","pred":"originalLabel","subj":"T27","obj":"D008181"},{"id":"A28","pred":"originalLabel","subj":"T28","obj":"D004198"},{"id":"A29","pred":"originalLabel","subj":"T29","obj":"D001172"},{"id":"A30","pred":"originalLabel","subj":"T30","obj":"D008180"},{"id":"A31","pred":"originalLabel","subj":"T31","obj":"D008181"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T8","span":{"begin":56,"end":60},"obj":"GeneOrGeneProduct"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T30","span":{"begin":29,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T32","span":{"begin":132,"end":134},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T34","span":{"begin":136,"end":139},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T35","span":{"begin":144,"end":146},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A30","pred":"mondo_id","subj":"T30","obj":"0002486"},{"id":"A31","pred":"mondo_id","subj":"T30","obj":"0005556"},{"id":"A32","pred":"mondo_id","subj":"T32","obj":"0008383"},{"id":"A33","pred":"mondo_id","subj":"T32","obj":"0005272"},{"id":"A34","pred":"mondo_id","subj":"T34","obj":"0007915"},{"id":"A35","pred":"mondo_id","subj":"T35","obj":"0002486"},{"id":"A36","pred":"mondo_id","subj":"T35","obj":"0005556"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T28","span":{"begin":29,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T29","span":{"begin":96,"end":118},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T30","span":{"begin":132,"end":134},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T31","span":{"begin":136,"end":139},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T32","span":{"begin":144,"end":146},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A28","pred":"ID:","subj":"T28","obj":"D008181"},{"id":"A29","pred":"ID:","subj":"T29","obj":"D004198"},{"id":"A30","pred":"ID:","subj":"T30","obj":"D001172"},{"id":"A31","pred":"ID:","subj":"T31","obj":"D008180"},{"id":"A32","pred":"ID:","subj":"T32","obj":"D008181"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T23","span":{"begin":29,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T24","span":{"begin":96,"end":118},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T25","span":{"begin":132,"end":134},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T26","span":{"begin":136,"end":139},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T27","span":{"begin":144,"end":146},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A23","pred":"#label","subj":"T23","obj":"D008181"},{"id":"A24","pred":"#label","subj":"T24","obj":"D004198"},{"id":"A25","pred":"#label","subj":"T25","obj":"D001172"},{"id":"A26","pred":"#label","subj":"T26","obj":"D008180"},{"id":"A27","pred":"#label","subj":"T27","obj":"D008181"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T8","span":{"begin":56,"end":60},"obj":"GeneOrGeneProduct"},{"id":"T27","span":{"begin":144,"end":146},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T26","span":{"begin":136,"end":139},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T25","span":{"begin":132,"end":134},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T24","span":{"begin":96,"end":118},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T23","span":{"begin":29,"end":31},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T32460","span":{"begin":61,"end":64},"obj":"SequenceVariant"}],"attributes":[{"id":"A27","pred":"#label","subj":"T27","obj":"D008181"},{"id":"A26","pred":"#label","subj":"T26","obj":"D008180"},{"id":"A25","pred":"#label","subj":"T25","obj":"D001172"},{"id":"A24","pred":"#label","subj":"T24","obj":"D004198"},{"id":"A23","pred":"#label","subj":"T23","obj":"D008181"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"DisGeNET","denotations":[{"id":"T2","span":{"begin":56,"end":60},"obj":"gene:1234"},{"id":"T3","span":{"begin":132,"end":134},"obj":"disease:C0003873"}],"relations":[{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"20682662-12#56#60#gene1234","span":{"begin":56,"end":60},"obj":"gene1234"},{"id":"20682662-12#132#134#diseaseC0003873","span":{"begin":132,"end":134},"obj":"diseaseC0003873"},{"id":"20682662-12#144#146#diseaseC0024143","span":{"begin":144,"end":146},"obj":"diseaseC0024143"}],"relations":[{"id":"56#60#gene1234132#134#diseaseC0003873","pred":"associated_with","subj":"20682662-12#56#60#gene1234","obj":"20682662-12#132#134#diseaseC0003873"},{"id":"56#60#gene1234144#146#diseaseC0024143","pred":"associated_with","subj":"20682662-12#56#60#gene1234","obj":"20682662-12#144#146#diseaseC0024143"}],"text":"Although an association with LN cannot be excluded, the CCR5 Δ32 deletion does not seem to be a disease susceptibility genotype for RA, SLE, or LN."}