@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk> .
@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:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_head {
  this: np:hasAssertion dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion;
    np:hasProvenance dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_provenance;
    np:hasPublicationInfo dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion a np:Assertion .
  
  dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_provenance a np:Provenance .
  
  dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion {
  miriam-gene:23562 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGNed1b2152d95c2df685c101478e33a4ad sio:SIO_000628 miriam-gene:23562, lld:C0581883;
    a sio:SIO_001121 .
}

dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_provenance {
  dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion dcterms:description
      "[The essential function of one of these claudins in the inner ear was established by identifying mutations in CLDN14 that cause nonsyndromic recessive deafness DFNB29 in two large consanguineous Pakistani families.]. 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:11163249;
    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:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:20+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" .
}