@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI> .
@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:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_head {
  this: np:hasAssertion dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_assertion;
    np:hasProvenance dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_provenance;
    np:hasPublicationInfo dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_assertion a np:Assertion .
  
  dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_provenance a np:Provenance .
  
  dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_assertion {
  miriam-gene:81622 a ncit:C16612 .
  
  lld:C0276226 a ncit:C7057 .
  
  dgn-gda:DGNdf05ebb334095078621ccb82205231b2 sio:SIO_000628 miriam-gene:81622, lld:C0276226;
    a sio:SIO_001121 .
}

dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_provenance {
  dgn-np:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_assertion dcterms:description
      "[Finally, mutations in UNC93B1 and TLR3 are associated with childhood herpes simplex encephalitis, which strikes only once in most patients, with almost no recorded cases of more than two bouts of this disease.]. 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:20236864;
    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:NP436378.RAiOaN3eq5T3y7LQRNJ8V3H8yJozeWpNb55_vq5Dco8zI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:18+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" .
}