@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_head {
  this: np:hasAssertion dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_assertion ;
    np:hasProvenance dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_provenance ;
    np:hasPublicationInfo dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_assertion a np:Assertion .
  dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_provenance a np:Provenance .
  dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_assertion {
  miriam-gene:4938 a ncit:C16612 .
  lld:C0026769 a ncit:C7057 .
  dgn-gda:DGN1307f1db20b852ea157919850e99a8d5 sio:SIO_000628 miriam-gene:4938 , lld:C0026769 ;
    a sio:SIO_001122 .
}
dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_provenance {
  dgn-np:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_assertion dcterms:description "[findings indicate that the OAS1 gene polymorphisms may confer susceptibility to multiple sclerosis or serve as markers of functional variants and suggest that OAS1 activity is involved in the etiology of the disease ]. 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:17092260 ;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP220759.RArgQVXgcKjTSVG_1s9DxmQi9RKprs3P_R4xwGpkhodv0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:26+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}