@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM> .
@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:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_head {
  this: np:hasAssertion dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion;
    np:hasProvenance dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_provenance;
    np:hasPublicationInfo dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion a np:Assertion .
  
  dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_provenance a np:Provenance .
  
  dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion {
  miriam-gene:5587 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN1d4d4a99a42abfb3cac811c01a264571 sio:SIO_000628 miriam-gene:5587, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_provenance {
  dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion dcterms:description
      "[Our clinical analysis, yet based only on a limited number of PKD2 subjects, does not definitely support the concept of a milder phenotype and prognosis in PKD2 versus PKD1 patients, in terms of mean age of diagnosis (29 vs. 29 years), mean age at onset of arterial hypertension (33 vs. 33 years), more favourable renal function or ultrasound findings.]. 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:9595261;
    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:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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" .
}