@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_head {
  this: np:hasAssertion dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_assertion;
    np:hasProvenance dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_provenance;
    np:hasPublicationInfo dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_assertion a np:Assertion .
  
  dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_provenance a np:Provenance .
  
  dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  
  lld:C0035078 a ncit:C7057 .
  
  dgn-gda:DGNe54892b1729e1d53eee50e213d780b8b sio:SIO_000628 miriam-gene:5243, lld:C0035078;
    a sio:SIO_001122 .
}

dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_provenance {
  dgn-np:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_assertion dcterms:description
      "[The purpose of this study is to compare the genotype frequency of C3435T and G1199A polymorphisms in MDR1 between ESRD patients and healthy controls in the Chinese population to determine whether the alteration of the P-gp function is associated with ESRD.]. 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:17376299;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP618361.RAHDvw7nvodPdR4zZR-yGTpAdG_VisehRn7LJ6Z2BDrCk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:49+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}