@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:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_head { this: np:hasAssertion dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_assertion; np:hasProvenance dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_provenance; np:hasPublicationInfo dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_publicationInfo; a np:Nanopublication . dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_assertion a np:Assertion . dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_provenance a np:Provenance . dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_publicationInfo a np:PublicationInfo . } dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_assertion { miriam-gene:1559 a ncit:C16612 . lld:C0024623 a ncit:C7057 . dgn-gda:DGN6b960b9959bdabfb36b21342907c2206 sio:SIO_000628 miriam-gene:1559, lld:C0024623; a sio:SIO_001122 . } dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_provenance { dgn-np:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_assertion dcterms:description "[ This is the first study to investigate a South American population for genetic polymorphism in the CYP2C subfamily. The Bolivian population differs from most other ethnic groups in the incidence of CYP2C9 and CYP2C19 common variants that might be influen]. 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:15776277; 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:NP91353.RApIss_Pg0libkMYx60Q-JJiCer5SO-pMhVkdt3hGVncw130_publicationInfo { this: dcterms:created "2016-05-13T12:42:29+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }