@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8> .
@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:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_head {
  this: np:hasAssertion dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_assertion;
    np:hasProvenance dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_provenance;
    np:hasPublicationInfo dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_assertion a np:Assertion .
  
  dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_provenance a np:Provenance .
  
  dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_assertion {
  miriam-gene:6277 a ncit:C16612 .
  
  lld:C0023895 a ncit:C7057 .
  
  dgn-gda:DGN46dc50234ee540b29c8d72a38b8da93f sio:SIO_000628 miriam-gene:6277, lld:C0023895;
    a sio:SIO_001121 .
}

dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_provenance {
  dgn-np:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_assertion dcterms:description
      "[Application of MboII PRA to samples from 241 Korean patients with chronic liver diseases of different clinical stages confirmed that F141L mutants were significantly related to HCC, even in comparison to liver cirrhosis (HCC, 26.3% of patients, or 26/99; liver cirrhosis, 3.8% of patients, or 2/52; P = 0.001).]. 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:20962085;
    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:NP428614.RAq4ceuAtbI3fJ6uLhGwqsRw1HwuuCcqpIC7MnGpoeaM8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:14+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: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" .
}