@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I> .
@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:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_head {
  this: np:hasAssertion dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion;
    np:hasProvenance dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance;
    np:hasPublicationInfo dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion a np:Assertion .
  
  dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance a np:Provenance .
  
  dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion {
  miriam-gene:57817 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGNe797b6e3c5fcb65309d3b285787c6525 sio:SIO_000628 miriam-gene:57817, lld:C0282193;
    a sio:SIO_001122 .
}

dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance {
  dgn-np:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion dcterms:description
      "[HJV p.A310G polymorphism and two intronic variants were found, but none of these alterations were associated with digenic inheritance with the HFE gene. Our data indicate that HJV and HAMP functional mutations are not frequent in these patients.]. 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:21039223;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:39+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" .
}