@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI> .
@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/v4.0.0/void/> .

dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_head {
  this: np:hasAssertion dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_assertion;
    np:hasProvenance dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_provenance;
    np:hasPublicationInfo dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_assertion a np:Assertion .
  
  dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_provenance a np:Provenance .
  
  dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_assertion {
  miriam-gene:1244 a ncit:C16612 .
  
  lld:C0268307 a ncit:C7057 .
  
  dgn-gda:DGNeb6e164388f99221988091051089babf sio:SIO_000628 miriam-gene:1244, lld:C0268307;
    a sio:SIO_001121 .
}

dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_provenance {
  dgn-np:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_assertion dcterms:description
      "[Pathophysiological consequences of many genetic variants leading to a lack of functional MRP protein in the plasma membrane are observed in the hereditary MRP2 deficiency associated with conjugated hyperbilirubinemia in Dubin-Johnson syndrome, in pseudoxanthoma elasticum due to mutations in the MRP6 (ABCC6) gene, or in the type of human earwax and osmidrosis determined by single nucleotide polymorphisms in the MRP8 (ABCC8) gene.]. 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:21103974;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP854326.RAGOBb5NwVNaBY3CoD8M9j_4YashQfreouK9DL1ma16VI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:12+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}