PubMed:9774399 / 0-266 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/9774399","sourcedb":"PubMed","sourceid":"9774399","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/9774399","text":"Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase.\nDefective NADPH oxidase components prevent superoxide (O-2) generation, causing chronic granulomatous disease (CGD). X-linked CGD patients have","tracks":[{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":133,"end":138},"obj":"gene:1666"},{"id":"T1","span":{"begin":203,"end":232},"obj":"disease:C0018203"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"attributes":[{"subj":"T0","pred":"source","obj":"DisGeNET"},{"subj":"T1","pred":"source","obj":"DisGeNET"}]},{"project":"DisGeNET5_gene_disease","denotations":[{"id":"9774399-1#10#15#gene1666","span":{"begin":133,"end":138},"obj":"gene1666"},{"id":"9774399-1#80#109#diseaseC0018203","span":{"begin":203,"end":232},"obj":"diseaseC0018203"},{"id":"9774399-1#111#114#diseaseC0018203","span":{"begin":234,"end":237},"obj":"diseaseC0018203"}],"relations":[{"id":"10#15#gene166680#109#diseaseC0018203","pred":"associated_with","subj":"9774399-1#10#15#gene1666","obj":"9774399-1#80#109#diseaseC0018203"},{"id":"10#15#gene1666111#114#diseaseC0018203","pred":"associated_with","subj":"9774399-1#10#15#gene1666","obj":"9774399-1#111#114#diseaseC0018203"}],"attributes":[{"subj":"9774399-1#10#15#gene1666","pred":"source","obj":"DisGeNET5_gene_disease"},{"subj":"9774399-1#80#109#diseaseC0018203","pred":"source","obj":"DisGeNET5_gene_disease"},{"subj":"9774399-1#111#114#diseaseC0018203","pred":"source","obj":"DisGeNET5_gene_disease"}]},{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":122},"obj":"Sentence"},{"id":"TextSentencer_T2","span":{"begin":123,"end":239},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":122},"obj":"Sentence"},{"id":"T2","span":{"begin":123,"end":239},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T1","pred":"source","obj":"sentences"},{"subj":"TextSentencer_T2","pred":"source","obj":"sentences"},{"subj":"T1","pred":"source","obj":"sentences"},{"subj":"T2","pred":"source","obj":"sentences"}]},{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":203,"end":232},"obj":"ORDO:379"},{"id":"AB2","span":{"begin":234,"end":237},"obj":"ORDO:379"},{"id":"AB3","span":{"begin":249,"end":252},"obj":"ORDO:379"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"attributes":[{"subj":"AB1","pred":"source","obj":"PubCasesORDO"},{"subj":"AB2","pred":"source","obj":"PubCasesORDO"},{"subj":"AB3","pred":"source","obj":"PubCasesORDO"}]},{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":203,"end":232},"obj":"Disease"},{"id":"T2","span":{"begin":234,"end":237},"obj":"Disease"},{"id":"T4","span":{"begin":249,"end":252},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0018305"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0010600"},{"id":"A3","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0018305"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0010600"},{"id":"A5","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0018305"},{"subj":"T1","pred":"source","obj":"mondo_disease"},{"subj":"T2","pred":"source","obj":"mondo_disease"},{"subj":"T4","pred":"source","obj":"mondo_disease"}]},{"project":"NCBITAXON","denotations":[{"id":"T1","span":{"begin":102,"end":107},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"9606"},{"subj":"T1","pred":"source","obj":"NCBITAXON"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"DisGeNET","color":"#b693ec","default":true},{"id":"DisGeNET5_gene_disease","color":"#93ec9c"},{"id":"sentences","color":"#ec93a3"},{"id":"PubCasesORDO","color":"#93bdec"},{"id":"mondo_disease","color":"#d7ec93"},{"id":"NCBITAXON","color":"#e693ec"}]}]}}