@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_head { this: np:hasAssertion dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_assertion; np:hasProvenance dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_provenance; np:hasPublicationInfo dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_publicationInfo; a np:Nanopublication . dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_assertion a np:Assertion . dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_provenance a np:Provenance . dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_publicationInfo a np:PublicationInfo . } dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_assertion { miriam-gene:1576 a ncit:C16612 . lld:C0023890 a ncit:C7057 . dgn-gda:DGNb6ef876f23bb36cdc12ae50ea5b2bc92 sio:SIO_000628 miriam-gene:1576, lld:C0023890; a sio:SIO_001121 . } dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_provenance { dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_assertion dcterms:description "[To study whether chronic liver disease (CLD) and genetic polymorphism affect the hepatic activity of cytochrome P450 (CYP) isoforms, we compared in vivo CYP2C19 and CYP3A activities using 3-hour omeprazole hydroxylation index (plasma concentration ratio of omeprazole to its 5-hydroxylated metabolite; a higher index indicates lower CYP2C19 activity) and partial formation clearance of cortisol to 6beta-hydroxycortisol (CL(cortisol-->6beta-HC)) in 31 CLD patients (9 with chronic hepatitis; 22 with cirrhosis comprising 20 Child-Pugh type A, 1 type B, and 1 type C) and 30 healthy subjects with different CYP2C19 genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:16239354; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP343495.RAg_EcTXpV8rpQduMGjbUtTV-d_V8UH2q_jCyaXSTdDwg130_publicationInfo { this: dcterms:created "2015-08-25T14:40:58+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }