@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_head {
  this: np:hasAssertion dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion;
    np:hasProvenance dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_provenance;
    np:hasPublicationInfo dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion a np:Assertion .
  
  dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_provenance a np:Provenance .
  
  dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C0155552 a ncit:C7057 .
  
  dgn-gda:DGNd8ec4aec299827fe280fbf5b95316632 sio:SIO_000628 miriam-gene:2706, lld:C0155552;
    a sio:SIO_001121 .
}

dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_provenance {
  dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion dcterms:description
      "[Based on these data, we hypothesize that Cx26 profound hearing loss may be not always congenital, with the possibility of an early window of functional time before the final defect is established.]. 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:17222463;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:12+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}