@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68> .
@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:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_head {
  this: np:hasAssertion dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion;
    np:hasProvenance dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_provenance;
    np:hasPublicationInfo dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion a np:Assertion .
  
  dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_provenance a np:Provenance .
  
  dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion {
  miriam-gene:4624 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGNac6038f84fa573811008721d72f001d3 sio:SIO_000628 miriam-gene:4624, lld:C0581883;
    a sio:SIO_001121 .
}

dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_provenance {
  dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion dcterms:description
      "[This loss of myosin VI function may not allow myosin VI to transport its cargoes appropriately at the base and within the stereocilia, or to anchor the membrane of stereocilia to actin filaments via its cargos, both of which lead to structural changes in the stereocilia of myosin VI-impaired hair cells, and ultimately leading to deafness.]. 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:18833301;
    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:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_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" .
}