@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ> .
@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:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_head {
  this: np:hasAssertion dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_assertion;
    np:hasProvenance dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_provenance;
    np:hasPublicationInfo dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_assertion a np:Assertion .
  
  dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_provenance a np:Provenance .
  
  dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_assertion {
  miriam-gene:2705 a ncit:C16612 .
  
  lld:C0031117 a ncit:C7057 .
  
  dgn-gda:DGN1e4133d567da3cfd187833b58a4e9215 sio:SIO_000628 miriam-gene:2705, lld:C0031117;
    a sio:SIO_001121 .
}

dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_provenance {
  dgn-np:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_assertion dcterms:description
      "[Our results indicate that 10 of 22 CMTX Cx32 mutations studied in the present investigation could lead to the assembly of defective Cx32 gap junctions, which in turn may result in peripheral 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-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:NP273826.RAUHnQreseyG1GD6Y7YMM_x8rjdrpMJl15nGVpNUzwIJQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:34+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" .
}