@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:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_head { this: np:hasAssertion dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_assertion; np:hasProvenance dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_provenance; np:hasPublicationInfo dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_publicationInfo; a np:Nanopublication . dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_assertion a np:Assertion . dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_provenance a np:Provenance . dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_publicationInfo a np:PublicationInfo . } dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_assertion { miriam-gene:1437 a ncit:C16612 . lld:C0275524 a ncit:C7057 . dgn-gda:DGN14bcaeee8f2a86bc814da2d07809af81 sio:SIO_000628 miriam-gene:1437, lld:C0275524; a sio:SIO_001121 . } dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_provenance { dgn-np:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_assertion dcterms:description "[(i) For HSV, 1/48 (2.1%, 86 copies/ml of CSF) MS patients and 1/23 (4.3%, 115.2 copies/ml of CSF) OIND patients (a myelitis case) had HSV sequences in the CSF; (ii) for EBV, only 1/48 (2.1%, 72 copies/ml of CSF) MS patients was positive for EBV; (iii) for HHV-6, only 5/48 (10.4%) MS patients had HHV-6 genomes in their CSF (128.1 copies/ml of CSF); (iv) we did not find any positive cases for VZV, CMV, HERV-H and HERV-W among MS patients or controls; (v) no cases of co-infections were found; (vi) the whole prevalence of HHVs was 7/48 (14.6%) for MS patients and 1/44 (2.3%) for controls (p = 0.038).]. 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:18566025; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP230320.RAbJnO1FcCX5pT_RDrDoUqCRxtopk3Nu7fc6TaILq8Uhc130_publicationInfo { this: dcterms:created "2014-10-02T12:34:09+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }