@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo> .
@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:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_head {
  this: np:hasAssertion dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion;
    np:hasProvenance dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_provenance;
    np:hasPublicationInfo dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion a np:Assertion .
  
  dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_provenance a np:Provenance .
  
  dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0011608 a ncit:C7057 .
  
  dgn-gda:DGN4e1e42193e46dc4248879c91dad2f29a sio:SIO_000628 miriam-gene:3133, lld:C0011608;
    a sio:SIO_001121 .
}

dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_provenance {
  dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion dcterms:description
      "[These findings suggest that the MHC susceptibility gene for DH is between class II and complotype regions, closest to the complotype, whereas that for GSE is in the class II region.]. 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:8245782;
    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:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}