@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ> .
@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:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_head {
  this: np:hasAssertion dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion;
    np:hasProvenance dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_provenance;
    np:hasPublicationInfo dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion a np:Assertion .
  
  dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_provenance a np:Provenance .
  
  dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion {
  miriam-gene:8718 a ncit:C16612 .
  
  lld:C0021053 a ncit:C7057 .
  
  dgn-gda:DGN853b39183b1e10d8232ac803fce7f68c sio:SIO_000628 miriam-gene:8718, lld:C0021053;
    a sio:SIO_001121 .
}

dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_provenance {
  dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion dcterms:description
      "[Based on these findings and those in other autoimmune diseases it is considered that the haplotype Bw46, DRw9 in Chinese takes the place of B8, DR3 in Caucasians in carrying genes which predispose to the development of auto-immune 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:3472422;
    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:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:45+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" .
}