PubMed:17003357 / 368-548 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/17003357","sourcedb":"PubMed","sourceid":"17003357","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/17003357","text":"In the current study, the haplotype structure of the PTPN22 region was determined, and individual haplotypes were tested for association with type 1 diabetes in family-based tests.","tracks":[{"project":"LitCoin-sentences","denotations":[{"id":"T4","span":{"begin":0,"end":180},"obj":"Sentence"}],"attributes":[{"subj":"T4","pred":"source","obj":"LitCoin-sentences"}]},{"project":"LitCoin-entities","denotations":[{"id":"3388","span":{"begin":53,"end":59},"obj":"GeneOrGeneProduct"},{"id":"3389","span":{"begin":142,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A10","pred":"db_id","subj":"3388","obj":"NCBIGene:26191"},{"id":"A11","pred":"db_id","subj":"3389","obj":"MESH:D003922"},{"subj":"3388","pred":"source","obj":"LitCoin-entities"},{"subj":"3389","pred":"source","obj":"LitCoin-entities"}],"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/"}]},{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T11","span":{"begin":53,"end":59},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":71,"end":81},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":114,"end":120},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":149,"end":157},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":168,"end":173},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":174,"end":179},"obj":"GeneOrGeneProduct"}],"attributes":[{"subj":"T11","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v0"},{"subj":"T12","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v0"},{"subj":"T13","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v0"},{"subj":"T14","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v0"},{"subj":"T15","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v0"},{"subj":"T16","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v0"}]},{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T8","span":{"begin":53,"end":59},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":149,"end":157},"obj":"GeneOrGeneProduct"}],"attributes":[{"subj":"T8","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v2"},{"subj":"T9","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v2"}]},{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T4","span":{"begin":142,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D003922"},{"subj":"T4","pred":"source","obj":"LitCoin-Disease-MeSH"}]},{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T5","span":{"begin":53,"end":59},"obj":"GeneOrGeneProduct"}],"attributes":[{"subj":"T5","pred":"source","obj":"LitCoin-GeneOrGeneProduct-v3"}]},{"project":"LitCoin_Mondo_095","denotations":[{"id":"T5","span":{"begin":142,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0005147"},{"subj":"T5","pred":"source","obj":"LitCoin_Mondo_095"}]},{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T4","span":{"begin":142,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"ID:","subj":"T4","obj":"D003922"},{"subj":"T4","pred":"source","obj":"LitCoin-MeSH-Disease-2"}]},{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T4","span":{"begin":142,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"#label","subj":"T4","obj":"D003922"},{"subj":"T4","pred":"source","obj":"LitCoin-MONDO_bioort2019"}]},{"project":"LitCoin-training-merged","denotations":[{"id":"T5","span":{"begin":53,"end":59},"obj":"GeneOrGeneProduct"},{"id":"T3469","span":{"begin":142,"end":157},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"#label","subj":"T3469","obj":"D003922"},{"subj":"T5","pred":"source","obj":"LitCoin-training-merged"},{"subj":"T3469","pred":"source","obj":"LitCoin-training-merged"}]},{"project":"DisGeNET","denotations":[{"id":"T6","span":{"begin":53,"end":59},"obj":"gene:26191"},{"id":"T7","span":{"begin":142,"end":157},"obj":"disease:C0011854"}],"relations":[{"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/"}],"attributes":[{"subj":"T6","pred":"source","obj":"DisGeNET"},{"subj":"T7","pred":"source","obj":"DisGeNET"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"LitCoin-sentences","color":"#c9ec93","default":true},{"id":"LitCoin-entities","color":"#ec93e3"},{"id":"LitCoin-GeneOrGeneProduct-v0","color":"#93ecdb"},{"id":"LitCoin-GeneOrGeneProduct-v2","color":"#ecc193"},{"id":"LitCoin-Disease-MeSH","color":"#a793ec"},{"id":"LitCoin-GeneOrGeneProduct-v3","color":"#98ec93"},{"id":"LitCoin_Mondo_095","color":"#ec93b2"},{"id":"LitCoin-MeSH-Disease-2","color":"#93ccec"},{"id":"LitCoin-MONDO_bioort2019","color":"#e7ec93"},{"id":"LitCoin-training-merged","color":"#d793ec"},{"id":"DisGeNET","color":"#93ecbd"}]}]}}