@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc> .
@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:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_head {
  this: np:hasAssertion dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion;
    np:hasProvenance dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_provenance;
    np:hasPublicationInfo dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion a np:Assertion .
  
  dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_provenance a np:Provenance .
  
  dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion {
  miriam-gene:4363 a ncit:C16612 .
  
  lld:C1864002 a ncit:C7057 .
  
  dgn-gda:DGN9ef635a61d110b4cafa14104c41ad5a6 sio:SIO_000628 miriam-gene:4363, lld:C1864002;
    a sio:SIO_001122 .
}

dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_provenance {
  dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion dcterms:description
      "[ The genotypic results observed show an ethnic difference in the frequencies of the MRP1 genetic polymorphisms between Japanese and Caucasians. Further studies are required to better understand the clinical consequences of the MRP1 genetic variants.]. 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:12856092;
    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:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_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" .
}