@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM> .
@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:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_head {
  this: np:hasAssertion dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_assertion;
    np:hasProvenance dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_provenance;
    np:hasPublicationInfo dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_assertion a np:Assertion .
  
  dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_provenance a np:Provenance .
  
  dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_assertion {
  miriam-gene:3115 a ncit:C16612 .
  
  lld:C0018213 a ncit:C7057 .
  
  dgn-gda:DGN24f13dc187c896ec63a7fd7b76aa43c5 sio:SIO_000628 miriam-gene:3115, lld:C0018213;
    a sio:SIO_001121 .
}

dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_provenance {
  dgn-np:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_assertion dcterms:description
      "[HLA-DPB1 polymorphisms were investigated in 217 members of 21 multiplex families of patients with Graves' disease, who had previously been haplotyped, using in vitro enzymatic DNA amplification and hybridization with sequence-specific oligonucleotide probes.]. 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:8088306;
    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:NP314592.RAAze_K_jtTAUy2u6dbNBJsphXmpXZGxFTGIjVRHgqyfM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:00+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" .
}