@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_head {
  this: np:hasAssertion dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion;
    np:hasProvenance dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_provenance;
    np:hasPublicationInfo dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion a np:Assertion .
  
  dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_provenance a np:Provenance .
  
  dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion {
  miriam-gene:5819 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN34c3ed3cef9731c0ad6b76f9cdb3f79c sio:SIO_000628 miriam-gene:5819, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_provenance {
  dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion dcterms:description
      "[the analysis of a very large data set suggests that genetic polymorphisms in PVRL2 may influence MS severity and supports the possibility that viral factors may contribute to the clinical course of MS, consistent with previous reports.]. 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:16738668;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}