@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8> .
@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:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_head {
  this: np:hasAssertion dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_assertion;
    np:hasProvenance dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_provenance;
    np:hasPublicationInfo dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_assertion a np:Assertion .
  
  dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_provenance a np:Provenance .
  
  dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C0155552 a ncit:C7057 .
  
  dgn-gda:DGNa0cd600e156b7234b795ea9954f2fd47 sio:SIO_000628 miriam-gene:2706, lld:C0155552;
    a sio:SIO_001121 .
}

dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_provenance {
  dgn-np:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_assertion dcterms:description
      "[GJB2 mutations will be of particular interest in combination with universal infant hearing screening programs, because it has been shown that early identification of hearing loss and early intervention are crucial for language development.]. 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:12053143;
    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:NP357220.RA9Y4Rk70Iin3sVA30ndawyNYzt8k-ynmhwlHH89ww0H8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:27+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" .
}