@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M> .
@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:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_head {
  this: np:hasAssertion dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_assertion;
    np:hasProvenance dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_provenance;
    np:hasPublicationInfo dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_assertion a np:Assertion .
  
  dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_provenance a np:Provenance .
  
  dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN7b0c7fb8a5b07088fd7d8745a1d60f1a sio:SIO_000628 miriam-gene:2706, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_provenance {
  dgn-np:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_assertion dcterms:description
      "[The high prevalence of profound deafness in the village is due to mutations in the Connexin 26 gene, while the relatively high frequency of Down syndrome is not explained by maternal age only.]. 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:20635393;
    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:NP869377.RAGWvN5M47ZsuCcNsIc0XD-JDCZtHhKLIrZsEcwzP1z4M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:51+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" .
}