@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4> .
@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:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_head {
  this: np:hasAssertion dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_assertion;
    np:hasProvenance dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_provenance;
    np:hasPublicationInfo dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_assertion a np:Assertion .
  
  dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_provenance a np:Provenance .
  
  dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_assertion {
  miriam-gene:25861 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGN241f590a2f12293a483c17bcc7689615 sio:SIO_000628 miriam-gene:25861, lld:C0581883;
    a sio:SIO_001121 .
}

dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_provenance {
  dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_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:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:19+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" .
}