@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE> .
@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:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_head {
  this: np:hasAssertion dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_assertion;
    np:hasProvenance dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_provenance;
    np:hasPublicationInfo dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_assertion a np:Assertion .
  
  dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_provenance a np:Provenance .
  
  dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_assertion {
  miriam-gene:5020 a ncit:C16612 .
  
  lld:C0011175 a ncit:C7057 .
  
  dgn-gda:DGN1c1844fa042d2f509a2a229659a70737 sio:SIO_000628 miriam-gene:5020, lld:C0011175;
    a sio:SIO_001121 .
}

dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_provenance {
  dgn-np:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_assertion dcterms:description
      "[Five unique stories explain: (i) the use of transcriptomics to identify genes involved in the response to physiological (dehydration) and pathological (hypertension) cues; (ii) the use of mass spectrometry for single-cell level identification of biological active peptides in the HNS, and to measure in vitro release; (iii) the use of transgenic lines that express fusion transgenes enabling (by cross-breeding) the generation of double transgenic lines that can be used to study vasopressin (AVP) and oxytocin (OXT) neurones in the HNS, as well as their neuroanatomy, electrophysiology and activation upon exposure to any given stimulus; (iv) the use of viral vectors to demonstrate that somato-dendritically released AVP plays an important role in cardiovascular homeostasis by binding to V1a receptors on local somata and dendrites; and (v) the use of virally-mediated optogenetics to dissect the role of OXT and AVP in the modulation of a wide variety of behaviours.]. 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:22448850;
    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:NP709398.RAYdf-KV0KFxmp9C48YoODalbTnV6BFMJPV1y6VIr9fsE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}