@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY> .
@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:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_head {
  this: np:hasAssertion dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion;
    np:hasProvenance dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_provenance;
    np:hasPublicationInfo dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion a np:Assertion .
  
  dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_provenance a np:Provenance .
  
  dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  
  lld:C0151746 a ncit:C7057 .
  
  dgn-gda:DGN5b369042aae77bbf5a6585b4248c838e sio:SIO_000628 miriam-gene:5243, lld:C0151746;
    a sio:SIO_001122 .
}

dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_provenance {
  dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion dcterms:description
      "[ Based on these results, we conclude that homozygosity for the ABCB1 2677T (S893) allele is associated with reduced risk of chronic renal dysfunction among liver transplantation patients receiving an immunosuppressive regimen containing CNIs.]. 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:14583679;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}