@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8> .
@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:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_head {
  this: np:hasAssertion dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion ;
    np:hasProvenance dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_provenance ;
    np:hasPublicationInfo dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion a np:Assertion .
  dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_provenance a np:Provenance .
  dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion {
  miriam-gene:551 a ncit:C16612 .
  lld:C0011847 a ncit:C7057 .
  dgn-gda:DGN1030867f00f1431af01ecddae64ae9e2 sio:SIO_000628 miriam-gene:551 , lld:C0011847 ;
    a sio:SIO_001122 .
}
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_provenance {
  dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion dcterms:description "[ Both mutations result in reduced AVP prohormone processing and secretion probably due to retention in the ER. This supports, at least partly, the hypothesis that the mutations lead to the production of a mutant hormone precursor that fails to fold and/or dimerize properly and, as a consequence, is retained by the ER protein quality control machinery. Perinuclear accumulation of the V67A prohormone outside the ER indicates that additional mechanisms could be involved.]. 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:14678298 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}