@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4> .
@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:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_head {
  this: np:hasAssertion dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion;
    np:hasProvenance dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_provenance;
    np:hasPublicationInfo dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion a np:Assertion .
  
  dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_provenance a np:Provenance .
  
  dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion {
  miriam-gene:3767 a ncit:C16612 .
  
  lld:C0018802 a ncit:C7057 .
  
  dgn-gda:DGN79e0840c2c9441c831b978d712d118b2 sio:SIO_000628 miriam-gene:3767, lld:C0018802;
    a sio:SIO_001122 .
}

dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_provenance {
  dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion dcterms:description
      "[The Kir6.2 E23K polymorphism in DCM patients of Han ethnicity may increase the risk of negative outcomes such as congestive heart failure and sudden cardiac death by affecting LVEDD and LAD.]. 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:24222218;
    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:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:49+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" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}