@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_head {
  this: np:hasAssertion dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_assertion;
    np:hasProvenance dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_provenance;
    np:hasPublicationInfo dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_assertion a np:Assertion .
  
  dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_provenance a np:Provenance .
  
  dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_assertion {
  miriam-gene:112476 a ncit:C16612 .
  
  lld:C1868682 a ncit:C7057 .
  
  dgn-gda:DGN74371022c84b107cb40e8c9a9e5f27e6 sio:SIO_000628 miriam-gene:112476, lld:C1868682;
    a sio:SIO_001121 .
}

dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_provenance {
  dgn-np:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_assertion dcterms:description
      "[Mutations in the gene PRRT2 were identified in several Chinese families with PKD, suggesting that the gene may also be responsible for ICCA and BFIE in families linked to the chromosome 16 locus.]. 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:23343561;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP963771.RAWy7Bve2Lr2nQk-vMODmCFrOOZeDEghpFrHIE0evIIGg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:29+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}