@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU> .
@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:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_head {
  this: np:hasAssertion dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_assertion;
    np:hasProvenance dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_provenance;
    np:hasPublicationInfo dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_assertion a np:Assertion .
  
  dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_provenance a np:Provenance .
  
  dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_assertion {
  miriam-gene:5311 a ncit:C16612 .
  
  lld:C0158683 a ncit:C7057 .
  
  dgn-gda:DGN3e92657101e8419003fdb2629ab92b41 sio:SIO_000628 miriam-gene:5311, lld:C0158683;
    a sio:SIO_001121 .
}

dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_provenance {
  dgn-np:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_assertion dcterms:description
      "[Dysequilibrium between TRPP2 and PRKCSH may lead to cyst formation in PCLD patients with PRKCSH mutations, and thereby account for the overlapping manifestations observed in PCLD and 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:19801576;
    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:NP721075.RA5m3A0TyRm257Lmrk9UmoB7QdeP3b9ec83CgApXb4tEU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:18+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" .
}