@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU> .
@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:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_head {
  this: np:hasAssertion dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_assertion;
    np:hasProvenance dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_provenance;
    np:hasPublicationInfo dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_assertion a np:Assertion .
  
  dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_provenance a np:Provenance .
  
  dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_assertion {
  miriam-gene:358 a ncit:C16612 .
  
  lld:C0085548 a ncit:C7057 .
  
  dgn-gda:DGN4b01b684fc9f3ac79f45c1dbf86f8347 sio:SIO_000628 miriam-gene:358, lld:C0085548;
    a sio:SIO_001121 .
}

dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_provenance {
  dgn-np:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_assertion dcterms:description
      "[Our data suggest that hepatic cystogenesis in autosomal recessive polycystic kidney disease may involve increased fluid accumulation because of overexpression and abnormal location of AQP1, CFTR, and AE2 in cystic cholangiocytes.]. 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:18988797;
    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:NP541357.RAoOSi1M5shfbxYnowSALC6MgzLY6adr1bLGBMCfBNWgU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:26+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" .
}