@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M> .
@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:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_head {
  this: np:hasAssertion dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion;
    np:hasProvenance dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_provenance;
    np:hasPublicationInfo dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion a np:Assertion .
  
  dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_provenance a np:Provenance .
  
  dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion {
  miriam-gene:551 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNc533e4abf1d90f1544657afc1e13cab7 sio:SIO_000628 miriam-gene:551, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_provenance {
  dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion dcterms:description
      "[Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) is an inherited disease caused by progressive degeneration of the magnocellular neurons of the hypothalamus leading to decreased ability to produce the hormone arginine vasopressin (AVP).]. 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:9360520;
    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:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:30+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" .
}