@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_head {
  this: np:hasAssertion dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion;
    np:hasProvenance dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance;
    np:hasPublicationInfo dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion a np:Assertion .
  
  dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance a np:Provenance .
  
  dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C1846647 a ncit:C7057 .
  
  dgn-gda:DGN56a148a5968305ec370efeeca7ce93df sio:SIO_000628 miriam-gene:2706, lld:C1846647;
    a sio:SIO_001122 .
}

dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance {
  dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion dcterms:description
      "[The Cx26 mutant W77R, which has been implicated in autosomal recessive deafness, also failed to form functional gap channels by itself but did not significantly interfere with the function of wildtype Cx26.]. 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:9856479;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:26+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}