@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak> .
@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:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_head {
  this: np:hasAssertion dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_assertion;
    np:hasProvenance dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_provenance;
    np:hasPublicationInfo dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_assertion a np:Assertion .
  
  dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_provenance a np:Provenance .
  
  dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_assertion {
  miriam-gene:5244 a ncit:C16612 .
  
  lld:C0268318 a ncit:C7057 .
  
  dgn-gda:DGN322074eb304a3797dbd6043ea920d9be sio:SIO_000628 miriam-gene:5244, lld:C0268318;
    a sio:SIO_001121 .
}

dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_provenance {
  dgn-np:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_assertion dcterms:description
      "[The cause of ICP remains elusive, but there is evidence that mutations in the canalicular ABC transporter phospholipid flippase (MDR3) and in the bile salt export pump (BSEP) can predispose for the development of ICP.]. 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:16890614;
    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:NP452649.RATQgtUUihZ40E7AwNQNY_8twtnGGxsznaD-cMevDgdak130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:30+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" .
}