@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ> .
@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:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_head {
   this: np:hasAssertion dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_assertion ;
    np:hasProvenance dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_assertion a np:Assertion .
  dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_provenance a np:Provenance .
  dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_assertion {
   miriam-gene:10205 a ncit:C16612 .
  lld:C1863752 a ncit:C7057 .
  dgn-gda:DGN0a9ea2f84700df8614c2c2123a5a86a1 sio:SIO_000628 miriam-gene:10205 , lld:C1863752 ;
    a sio:SIO_001121 .
}
dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_provenance {
   dgn-np:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_assertion dcterms:description "[Among them, 28 patients with isolated Mondini dysplasia (MD group), 50 patients with enlarged vestibular aqueduct with Mondini dysplasia (EVA with MD group), 50 patients with enlarged vestibular aqueduct without Mondini dysplasia (EVA group), and 16 patients with other types of inner ear malformations (IEM group) were identified.]. 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:21961810 ;
    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:NP331412.RAvQOcTnFlpcUm7sA2zmJpBWQi_f8YW2VmRVTrm910sBQ130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:15+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" .
}