@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo> .
@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:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_head {
  this: np:hasAssertion dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_assertion;
    np:hasProvenance dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_provenance;
    np:hasPublicationInfo dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_assertion a np:Assertion .
  
  dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_provenance a np:Provenance .
  
  dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C0741923 a ncit:C7057 .
  
  dgn-gda:DGN08c9bb56ad03ce41c53928e0bb5fd78c sio:SIO_000628 miriam-gene:3757, lld:C0741923;
    a sio:SIO_001121 .
}

dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_provenance {
  dgn-np:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_assertion dcterms:description
      "[Recent data showed that long QT syndrome (LQTS) patients with mutations in the pore region of the HERG (LQT2) gene have significantly higher risk of cardiac events than subjects with mutations in the non-pore region.]. 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:14678125;
    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:NP277986.RAe37SKbsfqZUhlGaEpbxnsDO_hPop_EjU9toK41AfBGo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:36+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" .
}