@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:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_head { this: np:hasAssertion dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_assertion; np:hasProvenance dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_provenance; np:hasPublicationInfo dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_publicationInfo; a np:Nanopublication . dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_assertion a np:Assertion . dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_provenance a np:Provenance . dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_publicationInfo a np:PublicationInfo . } dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_assertion { miriam-gene:1577 a ncit:C16612 . lld:C0019693 a ncit:C7057 . dgn-gda:DGN4f7cbf5e44533656b3a55c07d69f884d sio:SIO_000628 miriam-gene:1577, lld:C0019693; a sio:SIO_001122 . } dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_provenance { dgn-np:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_assertion dcterms:description "[Our study corroborates previous findings indicating that knowledge of CYP2B6 genetic status should be taken into account for an EFV treatment. Our results also constitute the first demonstration of the significant influence of CYP2B6 genetic polymorphisms]. 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:20860463; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP77346.RA5B9lJ1Le7Nv1FSPGohCB4ho8tP7gdgAPaK01GI5t7Do130_publicationInfo { this: dcterms:created "2015-08-25T14:38:22+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" . }