PubMed:9774399 / 507-741 JSONTXT

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"9774399-3#134#143#gene1536","span":{"begin":134,"end":143},"obj":"gene1536"},{"id":"9774399-3#31#34#diseaseC0018203","span":{"begin":31,"end":34},"obj":"diseaseC0018203"}],"relations":[{"id":"134#143#gene153631#34#diseaseC0018203","pred":"associated_with","subj":"9774399-3#134#143#gene1536","obj":"9774399-3#31#34#diseaseC0018203"}],"text":"We here report a rare X-linked CGD patient whose neutrophils entirely failed to produce O-2, but presented a diminished expression of gp91(phox) containing about one-third of the heme present in normal individuals by Soret absorption."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T4","span":{"begin":0,"end":234},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":234},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"We here report a rare X-linked CGD patient whose neutrophils entirely failed to produce O-2, but presented a diminished expression of gp91(phox) containing about one-third of the heme present in normal individuals by Soret absorption."}

{"project":"PubCasesORDO","denotations":[{"id":"AB4","span":{"begin":31,"end":34},"obj":"ORDO:379"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"We here report a rare X-linked CGD patient whose neutrophils entirely failed to produce O-2, but presented a diminished expression of gp91(phox) containing about one-third of the heme present in normal individuals by Soret absorption."}

{"project":"mondo_disease","denotations":[{"id":"T6","span":{"begin":31,"end":34},"obj":"Disease"}],"attributes":[{"id":"A6","pred":"mondo_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/MONDO_0010600"},{"id":"A7","pred":"mondo_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/MONDO_0018305"}],"text":"We here report a rare X-linked CGD patient whose neutrophils entirely failed to produce O-2, but presented a diminished expression of gp91(phox) containing about one-third of the heme present in normal individuals by Soret absorption."}

{"project":"NCBITAXON","denotations":[{"id":"T2","span":{"begin":35,"end":42},"obj":"OrganismTaxon"}],"attributes":[{"id":"A2","pred":"db_id","subj":"T2","obj":"9606"}],"text":"We here report a rare X-linked CGD patient whose neutrophils entirely failed to produce O-2, but presented a diminished expression of gp91(phox) containing about one-third of the heme present in normal individuals by Soret absorption."}

{"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":49,"end":60},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL_0000775"}],"text":"We here report a rare X-linked CGD patient whose neutrophils entirely failed to produce O-2, but presented a diminished expression of gp91(phox) containing about one-third of the heme present in normal individuals by Soret absorption."}

{"project":"CL-cell","denotations":[{"id":"T1","span":{"begin":49,"end":60},"obj":"Cell"}],"attributes":[{"id":"A1","pred":"cl_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL:0000775"}],"text":"We here report a rare X-linked CGD patient whose neutrophils entirely failed to produce O-2, but presented a diminished expression of gp91(phox) containing about one-third of the heme present in normal individuals by Soret absorption."}