@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4> .
@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:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_head {
  this: np:hasAssertion dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion;
    np:hasProvenance dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_provenance;
    np:hasPublicationInfo dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion a np:Assertion .
  
  dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_provenance a np:Provenance .
  
  dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion {
  miriam-gene:185 a ncit:C16612 .
  
  lld:C0042580 a ncit:C7057 .
  
  dgn-gda:DGN7cb7b8d8f418aebf903e7bd5e987b0f3 sio:SIO_000628 miriam-gene:185, lld:C0042580;
    a sio:SIO_001122 .
}

dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_provenance {
  dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion dct:description
      "[To detect the relation of the risk factors of primary VUR with the genetic polymorphism, the distribution of ACE, AT1 and AT2 genotypes after stratification by risk factors was also studied in the primary VUR patients.]. 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:14764974;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}