@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU> .
@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:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_head {
  this: np:hasAssertion dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_assertion;
    np:hasProvenance dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_provenance;
    np:hasPublicationInfo dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_assertion a np:Assertion .
  
  dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_provenance a np:Provenance .
  
  dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_assertion {
  miriam-gene:128368 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNa396aaabe48fecd51d8f73c07ef9e21e sio:SIO_000628 miriam-gene:128368, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_provenance {
  dgn-np:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_assertion dcterms:description
      "[The risk effect of EVI5 was further validated for the general MS population in an independent set of 1318 MS patients from the Canadian Collaborative Project on the Genetic Susceptibility to MS. On the basis of the transmission disequilibrium testing, a weak but significant risk effect was observed (OR 1.15; P=0.03 and OR 1.15; P=0.04).]. 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:18401352;
    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:NP649418.RAub6uSb01sfDlcOlM9s8LiSUk75eaEzawrvPBL0xRvmU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}