@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI> .
@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:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_head {
  this: np:hasAssertion dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion;
    np:hasProvenance dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_provenance;
    np:hasPublicationInfo dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion a np:Assertion .
  
  dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_provenance a np:Provenance .
  
  dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion {
  miriam-gene:5589 a ncit:C16612 .
  
  lld:C0022680 a ncit:C7057 .
  
  dgn-gda:DGN4f0e86034ecdd8ae4f8ff369efde64f0 sio:SIO_000628 miriam-gene:5589, lld:C0022680;
    a sio:SIO_001121 .
}

dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_provenance {
  dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion dcterms:description
      "[PCLD exhibits both autosomal or recessive dominant pattern of inheritance and is characterized by the progressive development of multiple cysts, isolated or associated with polycystic kidney disease, that appear more extensive in women.]. 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:20138815;
    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:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:51+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" .
}