@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA> .
@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:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_head {
  this: np:hasAssertion dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_assertion;
    np:hasProvenance dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_provenance;
    np:hasPublicationInfo dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_assertion a np:Assertion .
  
  dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_provenance a np:Provenance .
  
  dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_assertion {
  miriam-gene:25861 a ncit:C16612 .
  
  lld:C0231706 a ncit:C7057 .
  
  dgn-gda:DGN36b33c7b1c6f0836c116f994da497725 sio:SIO_000628 miriam-gene:25861, lld:C0231706;
    a sio:SIO_001121 .
}

dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_provenance {
  dgn-np:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_assertion dcterms:description
      "[The whirler (wi) mouse mutant, characterised by deafness and circling behaviour, maps to the corresponding region on the murine chromosome 4, thus suggesting that DFNB31 and whirler may result from orthologous gene defects.]. 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:11973626;
    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:NP226340.RA6_D_duzMWwShFH8xyCEzQuaCDjT2sdk2HswP2kyI2cA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:05+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" .
}