@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k> .
@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:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_head {
   this: np:hasAssertion dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_assertion ;
    np:hasProvenance dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_provenance ;
    np:hasPublicationInfo dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_assertion a np:Assertion .
  dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_provenance a np:Provenance .
  dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_assertion {
   miriam-gene:1811 a ncit:C16612 .
  lld:C0848676 a ncit:C7057 .
  dgn-gda:DGNce3082da5d91a14e36f819b496285be8 sio:SIO_000628 miriam-gene:1811 , lld:C0848676 ;
    a sio:SIO_001121 .
}
dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_provenance {
   dgn-np:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_assertion dcterms:description "[A prospective clinical and laboratory study among eight adult Finnish men with CLD revealed constant oligoasthenoteratozoospermia but normal spermatogenesis, high chloride and low pH in seminal plasma, and three spermatoceles, suggesting that male subfertility is a clinical manifestation of CLD and could be caused by an analogous defect in the epithelial Cl-/HCO3- and water transport, as described for the CLD intestine.]. 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:16412765 ;
    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:NP719402.RAWs2PvUQKPu7aT_zaIMnao5VmV49y48Ki4l7k9Y6X94k130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:17+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" .
}