@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o> .
@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:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_head {
  this: np:hasAssertion dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_assertion;
    np:hasProvenance dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_provenance;
    np:hasPublicationInfo dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_assertion a np:Assertion .
  
  dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_provenance a np:Provenance .
  
  dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_assertion {
  miriam-gene:5310 a ncit:C16612 .
  
  lld:C0085413 a ncit:C7057 .
  
  dgn-gda:DGNbf27983c7f72d57710675e0251639cdd sio:SIO_000628 miriam-gene:5310, lld:C0085413;
    a sio:SIO_001121 .
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dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_provenance {
  dgn-np:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_assertion dcterms:description
      "[Here we focus on autosomal dominant polycystic kidney disease, which is attributable to mutations in the PKD1 and PKD2 genes and which is characterized by perturbations of renal epithelial cell growth control, fluid transport, and morphogenesis.]. 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:21079243;
    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:NP852586.RAJwOULiJgsq6bpC9UsBNpMblZ37WfB1hz8f9Qeq25Z5o130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:11+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}