@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE> .
@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:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_head {
  this: np:hasAssertion dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_assertion;
    np:hasProvenance dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_provenance;
    np:hasPublicationInfo dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_assertion a np:Assertion .
  
  dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_provenance a np:Provenance .
  
  dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_assertion {
  miriam-gene:5587 a ncit:C16612 .
  
  lld:C0022680 a ncit:C7057 .
  
  dgn-gda:DGNc5765ab98156fa94738e57323aee8a7f sio:SIO_000628 miriam-gene:5587, lld:C0022680;
    a sio:SIO_001121 .
}

dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_provenance {
  dgn-np:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_assertion dcterms:description
      "[Prompted by the surprising observations that disruption of IFT genes in mice led to polycystic kidney disease (PKD) and that PKD proteins are present on the sensory cilia of Caenorhabditis elegans, researchers have made a direct connection between PKD and cilia.]. 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:15723088;
    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:NP237366.RARoXcdsMIyGaIDtj0NUJ-xcov5bu_QVjcEb722O-bgfE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}