@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA> .
@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:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_head {
  this: np:hasAssertion dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_assertion;
    np:hasProvenance dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_provenance;
    np:hasPublicationInfo dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_assertion a np:Assertion .
  
  dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_provenance a np:Provenance .
  
  dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_assertion {
  miriam-gene:30061 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNa41a10044b0107f1813000ce9efe1b93 sio:SIO_000628 miriam-gene:30061, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_provenance {
  dgn-np:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_assertion dcterms:description
      "[To understand the role of hemochromatosis and transferrin receptor system mutations in breast cancer, we analyzed 19 sequence variations at HFE, TFR1, TFR2, and FPN1 and compared genotype frequencies between cases and controls in a German population.]. 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:15894659;
    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:NP286683.RA6x0f_oULSP8clqHCkIRU_0hpEIMFSxRLsYhdj3AdqQA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:43+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" .
}