@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_head {
  this: np:hasAssertion dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_assertion;
    np:hasProvenance dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_provenance;
    np:hasPublicationInfo dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_assertion a np:Assertion .
  
  dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_provenance a np:Provenance .
  
  dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_assertion {
  miriam-gene:30061 a ncit:C16612 .
  
  lld:C0018995 a ncit:C7057 .
  
  dgn-gda:DGNa8cd74ad3b89dfbcacfd9fd739bb1040 sio:SIO_000628 miriam-gene:30061, lld:C0018995;
    a sio:SIO_001122 .
}

dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_provenance {
  dgn-np:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_assertion dcterms:description
      "[gene coding and flanking regions were sequenced and examined for mutations that might modulate the iron burden of individuals harboring the common mutant hemochromatosis HFE genotype or cause hemochromatosis independent of mutations in the HFE gene ]. 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:11783942;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP192908.RAZJ2lM1KTf5IKWdD3s2ga3oEwMcqiMCb6orNtqgMXtMI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:14+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}