@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_head {
  this: np:hasAssertion dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_assertion;
    np:hasProvenance dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_provenance;
    np:hasPublicationInfo dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_assertion a np:Assertion .
  
  dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_provenance a np:Provenance .
  
  dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_assertion {
  miriam-gene:6445 a ncit:C16612 .
  
  lld:C1563705 a ncit:C7057 .
  
  dgn-gda:DGNdebdf212148752d36da26a1b25153a3a sio:SIO_000628 miriam-gene:6445, lld:C1563705;
    a sio:SIO_001121 .
}

dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_provenance {
  dgn-np:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_assertion dcterms:description
      "[Recent elucidation of the vasopressin V2 (renal type) receptor gene structure has enabled us to test the hypothesis that the genetic defect in the V2 receptor is the likely molecular basis of NDI.]. 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:8267567;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP692493.RAPtAErCexDfF7sxw8VNconLM93KuFF4OXmd3Zvl7L1Lc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:37+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}