@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To> .
@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:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_head {
  this: np:hasAssertion dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_assertion;
    np:hasProvenance dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_provenance;
    np:hasPublicationInfo dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_assertion a np:Assertion .
  
  dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_provenance a np:Provenance .
  
  dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0392514 a ncit:C7057 .
  
  dgn-gda:DGNe3888006ece30d5ef21d68f471ff7713 sio:SIO_000628 miriam-gene:3077, lld:C0392514;
    a sio:SIO_001121 .
}

dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_provenance {
  dgn-np:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_assertion dcterms:description
      "[Identification of HFE, the gene most commonly mutated in patients with hereditary hemochromatosis, has allowed molecular diagnosis and paved the way for identification of other genes, such as TFR2, that are important in non-HFE-associated iron overload.]. 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:11673399;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP333975.RAuWQdSpMSMqrrf50_pkepqC0o3_wj5XfYgujhXJd_9To130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:16+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" .
}