@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA> .
@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:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_head {
  this: np:hasAssertion dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_assertion;
    np:hasProvenance dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_provenance;
    np:hasPublicationInfo dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_assertion a np:Assertion .
  
  dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_provenance a np:Provenance .
  
  dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNe87fe7c194d9b352f064128bb40ab5d1 sio:SIO_000628 miriam-gene:5265, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_provenance {
  dgn-np:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_assertion dcterms:description
      "[HFE and alpha-1 antitrypsin polymorphisms were characterized in 200 Egyptian patients with HCV infection (100 patients complicated with cirrhosis, 100 patients with HCC) and 100 healthy subjects who had no history of any malignancy.]. 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:21925577;
    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:NP387743.RAPAMTEgmOMh6RiE2qht3cFtPqgTVAGIo__ljxmduOBqA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}