@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I> .
@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:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_head {
  this: np:hasAssertion dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_assertion ;
    np:hasProvenance dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_provenance ;
    np:hasPublicationInfo dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_assertion a np:Assertion .
  dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_provenance a np:Provenance .
  dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_assertion {
  miriam-gene:7389 a ncit:C16612 .
  lld:C0019159 a ncit:C7057 .
  dgn-gda:DGN1b51f4323292430af45d1cc430aa3e09 sio:SIO_000628 miriam-gene:7389 , lld:C0019159 ;
    a sio:SIO_001121 .
}
dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_provenance {
  dgn-np:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_assertion dcterms:description "[Besides the epidemiological relevance of the association between PCT and hemochromatosis, however, it remains to be fully understood how iron overload, and in particular the cellular modifications of the iron status secondary to hemochromatosis mutations, affect the activity of URO-D, and how the altered iron metabolism interacts with the other two common triggers for PCT and etiological agents for the associated liver disease: alcohol and hepatitis viruses.]. 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:10189391 ;
    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:NP500322.RAIf_rIOpe7s-or6LQgVviKNphUwROejDWvELuVco52-I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:58+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" .
}