@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ> .
@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:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_head {
  this: np:hasAssertion dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_assertion;
    np:hasProvenance dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_provenance;
    np:hasPublicationInfo dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_assertion a np:Assertion .
  
  dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_provenance a np:Provenance .
  
  dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNd1ce3f7f3cf2bdd077ac2392f8157f81 sio:SIO_000628 miriam-gene:3106, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_provenance {
  dgn-np:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_assertion dcterms:description
      "[ The study strongly suggests the association among DR2, A23 and B21 allele and the evolution of ON to MS. High prevalence of A23 and DR2 alleles in CDMS patients compared with the normal population may suggest an important role for these alleles in the de]. 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:15471368;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP88362.RATQeiuAa7or6296Fc7vnR3dCu7NqBSRmP9Y3Nn7LiudQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:28+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" .
}