@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY> .
@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:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_head {
  this: np:hasAssertion dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_assertion;
    np:hasProvenance dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_provenance;
    np:hasPublicationInfo dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_assertion a np:Assertion .
  
  dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_provenance a np:Provenance .
  
  dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C1859062 a ncit:C7057 .
  
  dgn-gda:DGNecb82e025d4b2529fbea564ff37fda98 sio:SIO_000628 miriam-gene:3757, lld:C1859062;
    a sio:SIO_001121 .
}

dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_provenance {
  dgn-np:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_assertion dcterms:description
      "[In this review article, sympathetic stimulation with isoproterenol or epinephrine infusion is demonstrated to modulate differentially these repolarization indices in the ECG as well as the action potentials of the three cells between the LQT1, LQT2, and LQT3 syndromes both experimentally and clinically, explaining the differences in the sensitivity of genotypes of congenital LQTS to sympathetic stimulation.]. 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:12431311;
    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:NP390504.RAAytF_n5-DyFaK7daba8qPkYrcMD8JY12GtWzVvYVfoY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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" .
}