PubMed:17033686 / 116-387 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T2","span":{"begin":0,"end":271},"obj":"Sentence"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-entities","denotations":[{"id":"3450","span":{"begin":0,"end":27},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3451","span":{"begin":77,"end":81},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3452","span":{"begin":111,"end":115},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3453","span":{"begin":228,"end":233},"obj":"GeneOrGeneProduct"},{"id":"3454","span":{"begin":247,"end":251},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3455","span":{"begin":266,"end":270},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"db_id","subj":"3450","obj":"MESH:D038901"},{"id":"A6","pred":"db_id","subj":"3451","obj":"MESH:D038901"},{"id":"A7","pred":"db_id","subj":"3452","obj":"MESH:D038901"},{"id":"A8","pred":"db_id","subj":"3453","obj":"NCBIGene:10084"},{"id":"A9","pred":"db_id","subj":"3454","obj":"MESH:D038901"},{"id":"A10","pred":"db_id","subj":"3455","obj":"MESH:D038901"}],"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":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T5","span":{"begin":0,"end":8},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":64,"end":73},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":77,"end":81},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":91,"end":100},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":111,"end":115},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":168,"end":173},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":188,"end":197},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":228,"end":233},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":247,"end":251},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":266,"end":270},"obj":"GeneOrGeneProduct"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T3","span":{"begin":0,"end":8},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":77,"end":81},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":111,"end":115},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":228,"end":233},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":247,"end":251},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":266,"end":270},"obj":"GeneOrGeneProduct"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T4","span":{"begin":0,"end":27},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":64,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":91,"end":100},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D038901"},{"id":"A5","pred":"originalLabel","subj":"T5","obj":"D013577"},{"id":"A6","pred":"originalLabel","subj":"T6","obj":"D013577"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T2","span":{"begin":228,"end":233},"obj":"GeneOrGeneProduct"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T4","span":{"begin":9,"end":27},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":108,"end":110},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":235,"end":238},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":263,"end":265},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0001071"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0009735"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0012833"},{"id":"A7","pred":"mondo_id","subj":"T7","obj":"0009735"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T4","span":{"begin":0,"end":27},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":77,"end":81},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":111,"end":115},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":247,"end":251},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":266,"end":270},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"ID:","subj":"T4","obj":"D038901"},{"id":"A5","pred":"ID:","subj":"T5","obj":"DISEASE"},{"id":"A6","pred":"ID:","subj":"T6","obj":"DISEASE"},{"id":"A7","pred":"ID:","subj":"T7","obj":"DISEASE"},{"id":"A8","pred":"ID:","subj":"T8","obj":"DISEASE"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T4","span":{"begin":0,"end":27},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":77,"end":81},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":111,"end":115},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":247,"end":251},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":266,"end":270},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"#label","subj":"T4","obj":"D038901"},{"id":"A5","pred":"#label","subj":"T5","obj":"DISEASE"},{"id":"A6","pred":"#label","subj":"T6","obj":"DISEASE"},{"id":"A7","pred":"#label","subj":"T7","obj":"DISEASE"},{"id":"A8","pred":"#label","subj":"T8","obj":"DISEASE"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T2","span":{"begin":228,"end":233},"obj":"GeneOrGeneProduct"},{"id":"T44580","span":{"begin":266,"end":270},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T87219","span":{"begin":247,"end":251},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6556","span":{"begin":111,"end":115},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T59750","span":{"begin":77,"end":81},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T30956","span":{"begin":0,"end":27},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"#label","subj":"T44580","obj":"DISEASE"},{"id":"A7","pred":"#label","subj":"T87219","obj":"DISEASE"},{"id":"A6","pred":"#label","subj":"T6556","obj":"DISEASE"},{"id":"A5","pred":"#label","subj":"T59750","obj":"DISEASE"},{"id":"A4","pred":"#label","subj":"T30956","obj":"D038901"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":271},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":271},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":77,"end":81},"obj":"gene:1741"},{"id":"T1","span":{"begin":0,"end":27},"obj":"disease:C1136249"},{"id":"T2","span":{"begin":111,"end":115},"obj":"gene:1741"},{"id":"T3","span":{"begin":0,"end":27},"obj":"disease:C1136249"},{"id":"T4","span":{"begin":247,"end":251},"obj":"gene:1741"},{"id":"T5","span":{"begin":0,"end":27},"obj":"disease:C1136249"}],"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"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":0,"end":8},"obj":"HP_0001417"},{"id":"T2","span":{"begin":9,"end":27},"obj":"HP_0001249"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"17033686-1#77#81#gene1741","span":{"begin":77,"end":81},"obj":"gene1741"},{"id":"17033686-1#111#115#gene1741","span":{"begin":111,"end":115},"obj":"gene1741"},{"id":"17033686-1#228#233#gene10084","span":{"begin":228,"end":233},"obj":"gene10084"},{"id":"17033686-1#247#251#gene1741","span":{"begin":247,"end":251},"obj":"gene1741"},{"id":"17033686-1#266#270#gene1741","span":{"begin":266,"end":270},"obj":"gene1741"},{"id":"17033686-1#0#27#diseaseC1136249","span":{"begin":0,"end":27},"obj":"diseaseC1136249"}],"relations":[{"id":"77#81#gene17410#27#diseaseC1136249","pred":"associated_with","subj":"17033686-1#77#81#gene1741","obj":"17033686-1#0#27#diseaseC1136249"},{"id":"111#115#gene17410#27#diseaseC1136249","pred":"associated_with","subj":"17033686-1#111#115#gene1741","obj":"17033686-1#0#27#diseaseC1136249"},{"id":"228#233#gene100840#27#diseaseC1136249","pred":"associated_with","subj":"17033686-1#228#233#gene10084","obj":"17033686-1#0#27#diseaseC1136249"},{"id":"247#251#gene17410#27#diseaseC1136249","pred":"associated_with","subj":"17033686-1#247#251#gene1741","obj":"17033686-1#0#27#diseaseC1136249"},{"id":"266#270#gene17410#27#diseaseC1136249","pred":"associated_with","subj":"17033686-1#266#270#gene1741","obj":"17033686-1#0#27#diseaseC1136249"}],"text":"X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR."}