@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo> .
@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:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_head {
  this: np:hasAssertion dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_assertion ;
    np:hasProvenance dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_provenance ;
    np:hasPublicationInfo dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_assertion a np:Assertion .
  dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_provenance a np:Provenance .
  dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_assertion {
  miriam-gene:4852 a ncit:C16612 .
  lld:C0036572 a ncit:C7057 .
  dgn-gda:DGNb6b51c080b6b752f6ae4974fa2c2ec49 sio:SIO_000628 miriam-gene:4852 , lld:C0036572 ;
    a sio:SIO_001121 .
}
dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_provenance {
  dgn-np:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_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-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:NP595975.RAq4y3eJ7PSGG4Ut9YSjuEg-Rcf1N1zNzOWRkn0ohDeYo130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:36+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" .
}