@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck> .
@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:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_head {
  this: np:hasAssertion dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_assertion;
    np:hasProvenance dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_provenance;
    np:hasPublicationInfo dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_assertion a np:Assertion .
  
  dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_provenance a np:Provenance .
  
  dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_assertion {
  miriam-gene:25865 a ncit:C16612 .
  
  lld:C0010709 a ncit:C7057 .
  
  dgn-gda:DGN14efce45cf7603ec04d169e99ebac458 sio:SIO_000628 miriam-gene:25865, lld:C0010709;
    a sio:SIO_001121 .
}

dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_provenance {
  dgn-np:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_assertion dcterms:description
      "[In the former disease the diagnostic utility of renal ultrasound was determined, as was the prognostic impact of genotype, the role of the renin-angiotensin system in the pre-hypertensive phase, the potential for somatic mutations of the PKD2 gene, or the combination of mutations in the PKD1 and PKD2 genes, in single cells to induce cysts, and the demonstration that human transheterozygotes of PKD1 and -2 are not embryonically lethal.]. 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:12028433;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP856325.RAs2KTNIb7zkyZGsvLigSDal92oePZ2gIZtl2OzkpA5ck130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}