@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM> .
@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:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_head {
  this: np:hasAssertion dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_assertion;
    np:hasProvenance dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_provenance;
    np:hasPublicationInfo dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_assertion a np:Assertion .
  
  dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_provenance a np:Provenance .
  
  dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_assertion {
  miriam-gene:213 a ncit:C16612 .
  
  lld:C1845202 a ncit:C7057 .
  
  dgn-gda:DGN1163fc62153f7d32d3c7e95eca5d8a94 sio:SIO_000628 miriam-gene:213, lld:C1845202;
    a sio:SIO_001121 .
}

dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_provenance {
  dgn-np:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_assertion dcterms:description
      "[We performed a stimulation test with 1-desamino-D arginin vasopressin (dDAVP) 0·3 μg/kg of bodyweight in three patients (two hemizygous male and one heterozygous female) with NSIAD with R137C mutation and measured on the one hand the levels of vWF and fVIII and the other hand urine osmolality and albumin excretion (UAE).]. 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:21834801;
    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:NP872857.RApqiDapU0bfKmK9EJN_i9kKPyY_BLkh7-dGqI3Kk4JcM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:53+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" .
}