@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og> .
@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:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_head {
  this: np:hasAssertion dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_assertion;
    np:hasProvenance dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_provenance;
    np:hasPublicationInfo dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_assertion a np:Assertion .
  
  dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_provenance a np:Provenance .
  
  dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0019163 a ncit:C7057 .
  
  dgn-gda:DGN73cbd80f80fade3fef9aca592e4a3a15 sio:SIO_000628 miriam-gene:3077, lld:C0019163;
    a sio:SIO_001121 .
}

dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_provenance {
  dgn-np:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_assertion dcterms:description
      "[To evaluate the incidence and spectrum of HFE mutations and the relative frequency of the two main alleles of transferrin receptor in patients with PCT originating from southern France, and to evaluate the relationship of these genetic data with iron status, and with hepatitis B and C and human immunodeficiency virus (HIV) infections.]. 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:11260010;
    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:NP602697.RARSxoxCritQL3BkbOTYIZcfm4JwS8yW5dfMGe20C-2Og130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:02+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" .
}