@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds> .
@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:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_head {
  this: np:hasAssertion dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_assertion;
    np:hasProvenance dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_provenance;
    np:hasPublicationInfo dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_assertion a np:Assertion .
  
  dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_provenance a np:Provenance .
  
  dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_assertion {
  miriam-gene:2697 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGN7d7f32e9caa68e01d741ecae43c460b5 sio:SIO_000628 miriam-gene:2697, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_provenance {
  dgn-np:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_assertion dcterms:description
      "[These findings implicate somatic genetic defects of Cx43 as a potential cause of AF and support the paradigm that sporadic, nonfamilial cases of lone AF may arise from genetic mosaicism that creates heterogeneous coupling patterns, predisposing the tissue to reentrant arrhythmias.]. 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:20606116;
    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:NP270877.RAWY2E_IJpLp3sTjpiqoGj-5I5i83S195pMG89WQfF6Ds130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:31+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" .
}