@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c> .
@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:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_head {
  this: np:hasAssertion dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion;
    np:hasProvenance dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_provenance;
    np:hasPublicationInfo dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion a np:Assertion .
  
  dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_provenance a np:Provenance .
  
  dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion {
  miriam-gene:2694 a ncit:C16612 .
  
  lld:C2711227 a ncit:C7057 .
  
  dgn-gda:DGNdba74c5c37c745d6233f201af026db41 sio:SIO_000628 miriam-gene:2694, lld:C2711227;
    a sio:SIO_001121 .
}

dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_provenance {
  dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion dcterms:description
      "[The aim of this work was to assess the frequency of LS, its relationship with host and viral factors and to what extent it can influence the response to antiviral combination therapy with pegylated interferon (INF)+ribavirin in a group of patients with CHC from a single center.]. 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:17032413;
    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:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:11+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" .
}