@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g> .
@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:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_head {
  this: np:hasAssertion dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion;
    np:hasProvenance dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_provenance;
    np:hasPublicationInfo dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion a np:Assertion .
  
  dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_provenance a np:Provenance .
  
  dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  
  lld:C0001824 a ncit:C7057 .
  
  dgn-gda:DGN895d6c25120df0a8d6a204da386f4213 sio:SIO_000628 miriam-gene:3106, lld:C0001824;
    a sio:SIO_001121 .
}

dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_provenance {
  dgn-np:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_assertion dcterms:description
      "[The results obtained revealed significant differences between the agranulocytosis patients and the healthy population in the human lymphocyte antigen (HLA) allele frequencies, and in the degree and the frequency of chromosome aberrations.]. 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:8845862;
    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:NP701851.RATU6C-xrWERsZp-qsl7ouiVY05Z_ke_tizRviGGm1a9g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:06+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" .
}