@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo> .
@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 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:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_head {
  this: np:hasAssertion dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_assertion;
    np:hasProvenance dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_provenance;
    np:hasPublicationInfo dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_assertion a np:Assertion .
  
  dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_provenance a np:Provenance .
  
  dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_assertion {
  miriam-gene:7466 a ncit:C16612 .
  
  lld:C1833021 a ncit:C7057 .
  
  dgn-gda:DGN7551815db128c366d9c251727aed19b6 sio:SIO_000628 miriam-gene:7466, lld:C1833021;
    a sio:SIO_001122 .
}

dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_provenance {
  dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_assertion dc:description
      "[An LFSNHL locus has recently been assigned to chromosome 4p16, and mutations in WFS1, the causative gene for Wolfram syndrome, have been found to cause LFSNHL in families with DFNA6, DFNA14, or DFNA38.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:12181639;
    prov:wasDerivedFrom dgn-void:uniprot-20130724;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  
  dgn-void:uniprot-20130724 pav:importedOn "2013-07-24"^^xsd:date .
}

dgn-np:NP7083.RAfzFsPCZ7YM84b00Z6oD948i2W38783-fZuiJ8COB5Bo130_publicationInfo {
  this: dc:created "2014-10-02T12:32:01+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}