@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM> .
@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:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_head {
  this: np:hasAssertion dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_assertion;
    np:hasProvenance dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_provenance;
    np:hasPublicationInfo dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_assertion a np:Assertion .
  
  dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_provenance a np:Provenance .
  
  dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_assertion {
  miriam-gene:5310 a ncit:C16612 .
  
  lld:C0010709 a ncit:C7057 .
  
  dgn-gda:DGN4fee1f0982bd782199a3da6b8ce22d34 sio:SIO_000628 miriam-gene:5310, lld:C0010709;
    a sio:SIO_001121 .
}

dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_provenance {
  dgn-np:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_assertion dcterms:description
      "[The spectrum of germ-line mutations in both genes and the somatic mutations identified from individual PKD1 or PKD2 cysts indicate that loss of function of either PKD1 or PKD2 is the mechanism of cystogenesis in autosomal-dominant polycystic kidney disease.]. 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:11195048;
    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:NP459483.RAYIgUh1ZQtbr5WnwH_qCJ1AP1rMeywoR9UNVP2cMlsMM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:33+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" .
}