@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc> .
@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:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_head {
  this: np:hasAssertion dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_assertion;
    np:hasProvenance dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_provenance;
    np:hasPublicationInfo dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_assertion a np:Assertion .
  
  dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_provenance a np:Provenance .
  
  dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_assertion {
  miriam-gene:5020 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNc627ca85bcb8650ffe5551499c25007f sio:SIO_000628 miriam-gene:5020, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_provenance {
  dgn-np:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_assertion dcterms:description
      "[However, unlike the D1 receptor, the hypertension in D5 receptor null mice is caused by the increased activity of the sympathetic nervous system, apparently due to activation of oxytocin, V1 vasopressin, and non-NMDA receptors in the central nervous system.]. 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:17630951;
    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:NP187452.RAaMZ3DKv2RS8d2P8Xpp1v6ygXwLl1bOhbKUtnPwT5bkc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}