@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w> .
@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:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_head {
  this: np:hasAssertion dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion;
    np:hasProvenance dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_provenance;
    np:hasPublicationInfo dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion a np:Assertion .
  
  dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_provenance a np:Provenance .
  
  dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion {
  miriam-gene:4700 a ncit:C16612 .
  
  lld:C0392514 a ncit:C7057 .
  
  dgn-gda:DGN09c511744df994959af800357f3f66c3 sio:SIO_000628 miriam-gene:4700, lld:C0392514;
    a sio:SIO_001121 .
}

dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_provenance {
  dgn-np:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_assertion dcterms:description
      "[We evaluated 99 patients on chronic hemodialysis estimating their serum ferritin (SF) levels, transfusion rate, and prevalence of HLA A3, B7 and B14 alleles, which are considered to be more frequent in idiopathic hemochromatosis.]. 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:3226455;
    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:NP857109.RAVRDRUakw3oVThtsBJIgV6WyMHMQMGzdFW461z6Jia2w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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" .
}