@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs> .
@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/v4.0.0/void/> .

dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_head {
  this: np:hasAssertion dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion;
    np:hasProvenance dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_provenance;
    np:hasPublicationInfo dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion a np:Assertion .
  
  dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_provenance a np:Provenance .
  
  dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion {
  miriam-gene:4887 a ncit:C16612 .
  
  lld:C0036572 a ncit:C7057 .
  
  dgn-gda:DGN5a301a6d90336f7d2e5e6056bec55b77 sio:SIO_000628 miriam-gene:4887, lld:C0036572;
    a sio:SIO_001121 .
}

dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_provenance {
  dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion dcterms:description
      "[This concept is strongly supported by evidence that genetically modified rats overexpressing the NPY gene are less susceptible to seizures while deletion of NPY or Y2 receptor genes results in increased susceptibility to seizures.]. 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:15337376;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:12+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}