@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA> .
@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/v4.0.0/void/> .

dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_head {
  this: np:hasAssertion dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion;
    np:hasProvenance dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_provenance;
    np:hasPublicationInfo dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion a np:Assertion .
  
  dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_provenance a np:Provenance .
  
  dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion {
  miriam-gene:551 a ncit:C16612 .
  
  lld:C0677501 a ncit:C7057 .
  
  dgn-gda:DGN481bc4ca57ee165cb966cdbb5fd654a2 sio:SIO_000628 miriam-gene:551, lld:C0677501;
    a sio:SIO_001121 .
}

dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_provenance {
  dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion dcterms:description
      "[To investigate the association of mutations in the arginine vasopressin receptor type II (V2R) gene with congenital nephrogenic diabetes insipidus (CNDI) in the Japanese, we analyzed the V2R gene, located on the X chromosome, in three Japanese pedigrees with CNDI.]. 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:8766937;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:00+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}