@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI> .
@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 dcterms: <http://purl.org/dc/terms/> .
@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:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_head {
  this: np:hasAssertion dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion;
    np:hasProvenance dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_provenance;
    np:hasPublicationInfo dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion a np:Assertion .
  
  dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_provenance a np:Provenance .
  
  dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion {
  miriam-gene:2475 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGNe11b3e41d26807f38c2f5c4428608721 sio:SIO_000628 miriam-gene:2475, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_provenance {
  dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion dcterms:description
      "[Experiments with overactivation or disruption of key lifespan determinant pathways, such as silent information regulator (SIR)T1, p66Shc, and mammalian target of rapamycin (TOR), lead to development of features of the metabolic syndrome in mice.]. 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:21040402;
    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:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:49+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: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" .
}