PubMed:15200408 / 1857-2135 JSONTXT

{"project":"LitCoin-entities","denotations":[{"id":"923","span":{"begin":125,"end":134},"obj":"GeneOrGeneProduct"},{"id":"924","span":{"begin":180,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"925","span":{"begin":187,"end":193},"obj":"OrganismTaxon"}],"attributes":[{"id":"A37","pred":"db_id","subj":"923","obj":"NCBIGene:11045"},{"id":"A38","pred":"db_id","subj":"923","obj":"NCBIGene:7380"},{"id":"A39","pred":"db_id","subj":"924","obj":"MESH:C564042"},{"id":"A40","pred":"db_id","subj":"925","obj":"NCBITaxon:9606"}],"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":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-sentences","denotations":[{"id":"T16","span":{"begin":0,"end":278},"obj":"Sentence"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-entities-OrganismTaxon-PD","denotations":[{"id":"T5","span":{"begin":187,"end":193},"obj":"OrganismTaxon"}],"attributes":[{"id":"A5","pred":"db_id","subj":"T5","obj":"NCBItxid:9605"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T5","span":{"begin":80,"end":91},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0021152"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T42","span":{"begin":7,"end":11},"obj":"GeneOrGeneProduct"},{"id":"T43","span":{"begin":32,"end":36},"obj":"GeneOrGeneProduct"},{"id":"T44","span":{"begin":54,"end":60},"obj":"GeneOrGeneProduct"},{"id":"T45","span":{"begin":105,"end":113},"obj":"GeneOrGeneProduct"},{"id":"T46","span":{"begin":180,"end":183},"obj":"GeneOrGeneProduct"},{"id":"T47","span":{"begin":216,"end":220},"obj":"GeneOrGeneProduct"},{"id":"T48","span":{"begin":226,"end":233},"obj":"GeneOrGeneProduct"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T25","span":{"begin":7,"end":11},"obj":"GeneOrGeneProduct"},{"id":"T26","span":{"begin":32,"end":36},"obj":"GeneOrGeneProduct"},{"id":"T27","span":{"begin":180,"end":183},"obj":"GeneOrGeneProduct"},{"id":"T28","span":{"begin":216,"end":220},"obj":"GeneOrGeneProduct"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T18","span":{"begin":180,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T19","span":{"begin":270,"end":277},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A18","pred":"originalLabel","subj":"T18","obj":"D014718"},{"id":"A19","pred":"originalLabel","subj":"T19","obj":"D004194"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T27","span":{"begin":180,"end":183},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A27","pred":"mondo_id","subj":"T27","obj":"0008653"},{"id":"A28","pred":"mondo_id","subj":"T27","obj":"0006007"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T19","span":{"begin":180,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T20","span":{"begin":270,"end":277},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A19","pred":"ID:","subj":"T19","obj":"D014718"},{"id":"A20","pred":"ID:","subj":"T20","obj":"D004194"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T18","span":{"begin":180,"end":183},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A18","pred":"#label","subj":"T18","obj":"D014718"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T6","span":{"begin":187,"end":193},"obj":"OrganismTaxon"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T18","span":{"begin":180,"end":183},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T60905","span":{"begin":187,"end":193},"obj":"OrganismTaxon"}],"attributes":[{"id":"A18","pred":"#label","subj":"T18","obj":"D014718"}],"text":"Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease."}