@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro> .
@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:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_head {
  this: np:hasAssertion dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_assertion ;
    np:hasProvenance dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_provenance ;
    np:hasPublicationInfo dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_provenance a np:Provenance .
  dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_assertion {
  miriam-gene:161497 a ncit:C16612 .
  lld:C0011053 a ncit:C7057 .
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}
dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_provenance {
  dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_assertion dcterms:description "[We show how mouse models for nonsyndromic forms of deafness involving genes encoding Triobp and stereocilin reveal, respectively, the way stereocilia rootlets contribute to the hair bundle's mechanical properties and how the hair bundle produces suppressive masking, a property that contributes to speech intelligibility.]. 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:21073336 ;
    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 ;
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}
dgn-np:NP420280.RA_YtxAGd0p1tzQV2m8v_Ps84sSPtJzVQyZue_gSKxqro130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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> ;
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