@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q> .
@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:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_head {
  this: np:hasAssertion dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_assertion;
    np:hasProvenance dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_provenance;
    np:hasPublicationInfo dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_assertion a np:Assertion .
  
  dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_provenance a np:Provenance .
  
  dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_assertion {
  miriam-gene:5314 a ncit:C16612 .
  
  lld:C0085548 a ncit:C7057 .
  
  dgn-gda:DGN436cd2106d4c9c57e17318079c02b347 sio:SIO_000628 miriam-gene:5314, lld:C0085548;
    a sio:SIO_001122 .
}

dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_provenance {
  dgn-np:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_assertion dcterms:description
      "[These results suggest that the loss of fibrocystin may lead to abnormal proliferation in kidney epithelial cells and cyst formation in autosomal recessive polycystic kidney disease by modulation of intracellular Ca (2+).]. 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:17669261;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP152464.RAjTjSpc8XP36C3jSfjbOaLDAJI-8cutORSSH7HaM1I9Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:21+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" .
}