@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro> .
@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:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_head {
  this: np:hasAssertion dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion;
    np:hasProvenance dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_provenance;
    np:hasPublicationInfo dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion a np:Assertion .
  
  dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_provenance a np:Provenance .
  
  dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion {
  miriam-gene:159 a ncit:C16612 .
  
  lld:C0019348 a ncit:C7057 .
  
  dgn-gda:DGN46ac695a2c24f3c0a162b182839366dc sio:SIO_000628 miriam-gene:159, lld:C0019348;
    a sio:SIO_001121 .
}

dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_provenance {
  dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion dcterms:description
      "[Our findings suggest that distinct markers in IRF2 may be associated with AD and ADEH, which may depend upon ethnic ancestry, and genetic variants in IRF2 may contribute to an abnormal immune response to HSV.]. 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:22113474;
    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:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:18+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" .
}