@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8> .
@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:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_head {
  this: np:hasAssertion dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion;
    np:hasProvenance dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_provenance;
    np:hasPublicationInfo dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion a np:Assertion .
  
  dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_provenance a np:Provenance .
  
  dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion {
  miriam-gene:6550 a ncit:C16612 .
  
  lld:C0037859 a ncit:C7057 .
  
  dgn-gda:DGN241f3578f11e7994d22c7d0c199010f1 sio:SIO_000628 miriam-gene:6550, lld:C0037859;
    a sio:SIO_001121 .
}

dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_provenance {
  dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion dcterms:description
      "[Tissue-specific co-expression with CFTR and NHE3 supports diverse functions of SLC26A3 and may have an impact on pathophysiology of male subfertility both in CLD and in cystic fibrosis (CF), as well as spermatoceles.]. 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:16421216;
    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:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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" .
}