@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs> .
@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:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_head {
  this: np:hasAssertion dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion;
    np:hasProvenance dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_provenance;
    np:hasPublicationInfo dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion a np:Assertion .
  
  dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_provenance a np:Provenance .
  
  dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion {
  miriam-gene:8797 a ncit:C16612 .
  
  lld:C0007137 a ncit:C7057 .
  
  dgn-gda:DGNecd89d4121fda08c15d040bd1d43dc97 sio:SIO_000628 miriam-gene:8797, lld:C0007137;
    a sio:SIO_001121 .
}

dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_provenance {
  dgn-np:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_assertion dcterms:description
      "[There were significant differences in the frequencies of HLA DR1, DR4 and DR7 between patients who only had basal cell carcinomas and patients who had both basal and squamous cell carcinomas.]. 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:8136554;
    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:NP781780.RARTty37auH1hSK9v_rv4vloZwCaidKuc2Wyw_tNRLeOs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:53+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" .
}