@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A> .
@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:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_head {
  this: np:hasAssertion dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion ;
    np:hasProvenance dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_provenance ;
    np:hasPublicationInfo dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion a np:Assertion .
  dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_provenance a np:Provenance .
  dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  lld:C0003537 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_provenance {
  dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion dcterms:description "[Eight children with cochlear implants were subjected to genetic testing for GJB2 and underwent the Raven colored progressive matrices test, Rey's auditory verbal learning test, Rey's complex figure test, the standardized language test for aphasia, the picture vocabulary test, and the standardized comprehension test for abstract words.]. 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:16549217 ;
    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:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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 ;
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}