@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU> .
@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:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_head {
  this: np:hasAssertion dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_assertion ;
    np:hasProvenance dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_provenance ;
    np:hasPublicationInfo dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_assertion a np:Assertion .
  dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_provenance a np:Provenance .
  dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_assertion {
  miriam-gene:23562 a ncit:C16612 .
  lld:C0581883 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_provenance {
  dgn-np:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_assertion dcterms:description "[In order to identify the contribution of CLDN14 to less than profound deafness, we screened for mutations of CLDN14 in 30 multiplex and 57 sporadic cases with moderately severe to severe HL from Pakistan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP559178.RASmCtOLVT0waZUvJUYKr2kyaEn1hhSPW3ttkJTPk2qOU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:37+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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