@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA> .
@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:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_head {
  this: np:hasAssertion dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_assertion;
    np:hasProvenance dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_provenance;
    np:hasPublicationInfo dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_assertion a np:Assertion .
  
  dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_provenance a np:Provenance .
  
  dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_assertion {
  miriam-gene:10060 a ncit:C16612 .
  
  lld:C0018801 a ncit:C7057 .
  
  dgn-gda:DGN87b7ae219015cdaf23d624b223085b6d sio:SIO_000628 miriam-gene:10060, lld:C0018801;
    a sio:SIO_001121 .
}

dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_provenance {
  dgn-np:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_assertion dcterms:description
      "[Scanning of genomic DNA from individuals with heart failure and rhythm disturbances due to idiopathic dilated cardiomyopathy identified two mutations in ABCC9, which encodes the regulatory SUR2A subunit of the cardiac K(ATP) channel.]. 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:15034580;
    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:NP198810.RADagweVvaLtjfHVoKQ30SndlxX67hmqYjfCw8VALxgaA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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: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" .
}