@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E> .
@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:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_head {
  this: np:hasAssertion dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion ;
    np:hasProvenance dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_provenance ;
    np:hasPublicationInfo dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion a np:Assertion .
  dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_provenance a np:Provenance .
  dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion {
  miriam-gene:1351 a ncit:C16612 .
  lld:C0011053 a ncit:C7057 .
  dgn-gda:DGN156d4edd0c66e5ae1195fbce42acac45 sio:SIO_000628 miriam-gene:1351 , lld:C0011053 ;
    a sio:SIO_001121 .
}
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_provenance {
  dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion dcterms:description "[Inclusion criteria for this study were hearing loss of more than 30 dB hearing level affecting at least 3 contiguous frequencies, normal hearing on the contralateral ear, negative history of hearing loss or ear surgery in the affected ear, and magnetic resonance with gadolinium negative for VIII cranial nerve pathologic findings.]. 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:18401280 ;
    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:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:24+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" .
}