@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:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_head { this: np:hasAssertion dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_assertion; np:hasProvenance dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_provenance; np:hasPublicationInfo dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_publicationInfo; a np:Nanopublication . dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_assertion a np:Assertion . dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_provenance a np:Provenance . dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_publicationInfo a np:PublicationInfo . } dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_assertion { miriam-gene:4864 a ncit:C16612 . lld:C1827377 a ncit:C7057 . dgn-gda:DGN2e4df14897567220568484238c765c4f sio:SIO_000628 miriam-gene:4864, lld:C1827377; a sio:SIO_001121 . } dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_provenance { dgn-np:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_assertion dcterms:description "[The slow acetylator genotype remained considerably more common among FPD (73%) than normal control subjects (NPC, 43%) or the disease (Huntington's disease [HD]) control group (52%) with an odds ratio (OR) of 3.58 (95% confidence interval (CI): 1.96-6.56; p = 0.00003) for FPD versus NPC and an OR of 2.50 (95% CI: 1.37-4.56, p = 0.003) for FPD versus HD.]. 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:10634239; 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:NP597266.RAnRXatYhSrM2F02VicOMM9XUTlClcUuT1ueEKmZuglIs130_publicationInfo { this: dcterms:created "2015-08-25T14:43:37+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" . }