@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA> .
@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/v3.0.0/void/> .
dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_head {
   this: np:hasAssertion dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_assertion ;
    np:hasProvenance dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_provenance ;
    np:hasPublicationInfo dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_assertion a np:Assertion .
  dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_provenance a np:Provenance .
  dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_assertion {
   miriam-gene:10804 a ncit:C16612 .
  lld:C0022596 a ncit:C7057 .
  dgn-gda:DGNd354bfd14b6cc0c745bee49e487f000e sio:SIO_000628 miriam-gene:10804 , lld:C0022596 ;
    a sio:SIO_001122 .
}
dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_provenance {
   dgn-np:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_assertion dcterms:description "[HeLa cells stably expressing nine dominant Cx26 mutants, six associated with non-syndromic hearing loss (W44C, W44S, R143Q, D179N, R184Q and C202F) and three associated with hearing loss and palmoplantar keratoderma (G59A, R75Q and R75W), individually or together with Cx30, were analyzed by immunocytochemistry, co-immunoprecipitation, and functional assays (scrape-loading and/or fluorescence recovery after photobleaching).]. 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:20096356 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP853320.RAXC4s18Zax_EDk1oy5vdChWbIUIZwuWU5TjKFXQoFVRA130_publicationInfo {
   this: dcterms:created "2015-08-25T14:46:18+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 "v3.0.0.0" .
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}