@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA> .
@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:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_head {
  this: np:hasAssertion dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_assertion;
    np:hasProvenance dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_provenance;
    np:hasPublicationInfo dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_assertion a np:Assertion .
  
  dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_provenance a np:Provenance .
  
  dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_assertion {
  miriam-gene:3358 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_provenance {
  dgn-np:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_assertion dcterms:description
      "[We conclude that genetic variation in 5HTR2C may be associated with HPA axis activation and stimulated by emotional stress, and also with both psychological and physiological endophenotypes that increase the risk of cardiovascular disease and type-2 diabetes.]. 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:21967853;
    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:NP929056.RANOED72dBXRLHnC2TRCRXi3ecr5RC11hAzafEuUEFHnA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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