@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo> .
@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 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:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_head {
  this: np:hasAssertion dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_assertion;
    np:hasProvenance dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_provenance;
    np:hasPublicationInfo dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_assertion a np:Assertion .
  
  dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_provenance a np:Provenance .
  
  dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_assertion {
  miriam-gene:28996 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGN6dec5e8ac2c45377df353a2f4cb1f085 sio:SIO_000628 miriam-gene:28996, lld:C0022658;
    a sio:SIO_001121 .
}

dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_provenance {
  dgn-np:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_assertion dc:description
      "[In the light of promissing data concerning homeodomain-interacting protein kinase 2 (HIPK2) upregulation in damaged kidneys animal model, and increased levels of this protein in patients with various kidney diseases, the influence of rs7456421 and rs 2030712 single nucleotide polimorphisms of HIPK2 gene on chronic kidney disease incidence and progression was studied.]. 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:23540226;
    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:NP376703.RABdTLw5jbRb0D9mnCVB2gZZC19MEfH-9J0JflU2Tmejo130_publicationInfo {
  this: dc:created "2014-10-02T12:35:40+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}