@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8> .
@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:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_head {
  this: np:hasAssertion dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion;
    np:hasProvenance dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_provenance;
    np:hasPublicationInfo dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion a np:Assertion .
  
  dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_provenance a np:Provenance .
  
  dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion {
  miriam-gene:359 a ncit:C16612 .
  
  lld:C0162283 a ncit:C7057 .
  
  dgn-gda:DGNde32f1879cfa69a7b8f00932f6289bce sio:SIO_000628 miriam-gene:359, lld:C0162283;
    a sio:SIO_001121 .
}

dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_provenance {
  dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion dcterms:description
      "[In this article, we review the current understanding of the known genetic causes of nephrogenic diabetes insipidus that affect the binding of vasopressin to the V2 receptor and subsequent intracellular signaling events, as well as the translocation of aquaporin-2 water channels to the apical membrane.]. 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:14586738;
    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:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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" .
}