@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g> .
@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:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_head {
  this: np:hasAssertion dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_assertion;
    np:hasProvenance dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_provenance;
    np:hasPublicationInfo dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_assertion a np:Assertion .
  
  dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_provenance a np:Provenance .
  
  dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  
  lld:C0018133 a ncit:C7057 .
  
  dgn-gda:DGNf53497fae3e54c7289f8ad6edeb43a0d sio:SIO_000628 miriam-gene:5243, lld:C0018133;
    a sio:SIO_001122 .
}

dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_provenance {
  dgn-np:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_assertion dcterms:description
      "[This is the first report of the association of a drug disposition genotype with drug-resistant acute rejection in organ transplant patients. The major predictor of acute persistent rejection in the first postoperative year for lung transplant patients was the MDR1 C3435T genotype. This association could be due to drug resistance, altered drug disposition or other immunologic effects associated with P-glycoprotein (P-gp) function. Future prospective treatment algorithms should be developed that will incorporate the knowledge of gene polymorphisms into treatment regimens to improve the outcome following lung transplantation.]. 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:15814280;
    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:NP49781.RAVGsTd0f9wap4uESjF433ZIWuBTJlG-KieF5rOquDS4g130_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" .
}