@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y> .
@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:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_head {
  this: np:hasAssertion dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion;
    np:hasProvenance dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_provenance;
    np:hasPublicationInfo dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion a np:Assertion .
  
  dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_provenance a np:Provenance .
  
  dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion {
  miriam-gene:8647 a ncit:C16612 .
  
  lld:C0019196 a ncit:C7057 .
  
  dgn-gda:DGN0cc3d9f3b8cbbd808de27264b37bba6f sio:SIO_000628 miriam-gene:8647, lld:C0019196;
    a sio:SIO_001121 .
}

dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_provenance {
  dgn-np:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_assertion dcterms:description
      "[A common variant of BSEP (p.V444A) is now a well-established susceptibility factor for acquired cholestasis and recent evidence suggests that the same variant also influences the therapeutic response and disease progression of viral hepatitis C. Studies in large independent cohorts are now needed to confirm the relevance of p.V444A.]. 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:21320040;
    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:NP876879.RAAYX_gr7b-YrddTcvCMBbus9MLqbMIheefSyIpva5x3Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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" .
}