@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA> .
@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:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_head {
  this: np:hasAssertion dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_assertion;
    np:hasProvenance dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_provenance;
    np:hasPublicationInfo dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_assertion a np:Assertion .
  
  dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_provenance a np:Provenance .
  
  dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0276623 a ncit:C7057 .
  
  dgn-gda:DGN2ce446a7bce0fe35ee27a177a34b1ed2 sio:SIO_000628 miriam-gene:3077, lld:C0276623;
    a sio:SIO_001122 .
}

dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_provenance {
  dgn-np:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_assertion dcterms:description
      "[It is less well established that the prevalence of the HFE mutations is increased in alcoholic liver disease and in chronic viral hepatitis, but in both conditions, patients harboring one of these mutations, especially C282Y, are more likely to have advanced hepatic fibrosis or cirrhosis.]. 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:10980924;
    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:NP294663.RAPMJoOjEquVTX_dEmNFXqZHexWIoF2s19d-p4VNLe5QA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:59+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" .
}