@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_head {
  this: np:hasAssertion dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_assertion;
    np:hasProvenance dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_provenance;
    np:hasPublicationInfo dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_assertion a np:Assertion .
  
  dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_provenance a np:Provenance .
  
  dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_assertion {
  miriam-gene:5172 a ncit:C16612 .
  
  lld:C0155552 a ncit:C7057 .
  
  dgn-gda:DGN1525d64d55b5a8012c4fc93fbdfd3323 sio:SIO_000628 miriam-gene:5172, lld:C0155552;
    a sio:SIO_001121 .
}

dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_provenance {
  dgn-np:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_assertion dcterms:description
      "[Genomic techniques such as the polymerase chain reaction, linkage analysis, Sanger sequencing, and most recently, massively parallel sequencing, have allowed researchers and clinicians to identify mutations for patients with Pendred syndrome and DFNB4 non-syndromic hearing loss.]. 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:22116368;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP941733.RApolLKo7QXAtYkOCYIoF7KCaz7QuVuloNwu5lsnRXtdI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:52+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}