@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o> .
@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:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_head {
  this: np:hasAssertion dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_assertion;
    np:hasProvenance dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_provenance;
    np:hasPublicationInfo dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_assertion a np:Assertion .
  
  dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_provenance a np:Provenance .
  
  dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_assertion {
  miriam-gene:2705 a ncit:C16612 .
  
  lld:C0270922 a ncit:C7057 .
  
  dgn-gda:DGN1de43e73de728056e318382f5f24e28f sio:SIO_000628 miriam-gene:2705, lld:C0270922;
    a sio:SIO_001121 .
}

dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_provenance {
  dgn-np:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_assertion dcterms:description
      "[However, further studies are required to elucidate the exact mechanism by which CMTX mutant Cx32 proteins, which retain the ability to form homotypic junctional channels, damage Schwann cells and cause demyelinating neuropathy.]. 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:15006706;
    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:NP434580.RAiZb-0GPO3oH4QNOM5qiVvdAWBWXtszxPNzdKbyaYw0o130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:02+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" .
}