@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU> .
@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:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_head {
  this: np:hasAssertion dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion;
    np:hasProvenance dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_provenance;
    np:hasPublicationInfo dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion a np:Assertion .
  
  dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_provenance a np:Provenance .
  
  dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C3241937 a ncit:C7057 .
  
  dgn-gda:DGN083d76f5717e431f4d4a4461cedd4617 sio:SIO_000628 miriam-gene:3630, lld:C3241937;
    a sio:SIO_001121 .
}

dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_provenance {
  dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion dcterms:description
      "[Serum ferritin concentrations were measured in 86 patients with histopathologically verified NAFLD (24 with steatosis and 62 with NASH) and 20 control subjects, they were tested for HFE gene mutations and their insulin resistance was measured.]. 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:19267193;
    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:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}