@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs> .
@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:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_head {
  this: np:hasAssertion dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion;
    np:hasProvenance dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_provenance;
    np:hasPublicationInfo dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion a np:Assertion .
  
  dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_provenance a np:Provenance .
  
  dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion {
  miriam-gene:115352 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNac19b77664381ec3e6207e050fd678a7 sio:SIO_000628 miriam-gene:115352, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_provenance {
  dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion dcterms:description
      "[An increased susceptibility associated to the -169 T allele was found when MS patients and controls were compared, supporting the role of the FcRL3 locus in MS predisposition and therefore extending the evidence of its general influence on autoimmunity.]. 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:17617473;
    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:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}