@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA> .
@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:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_head {
  this: np:hasAssertion dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_assertion;
    np:hasProvenance dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_provenance;
    np:hasPublicationInfo dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_assertion a np:Assertion .
  
  dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_provenance a np:Provenance .
  
  dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_assertion {
  miriam-gene:27352 a ncit:C16612 .
  
  lld:C1631597 a ncit:C7057 .
  
  dgn-gda:DGN76324c83b610ecad56aede89e659f237 sio:SIO_000628 miriam-gene:27352, lld:C1631597;
    a sio:SIO_001121 .
}

dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_provenance {
  dgn-np:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_assertion dcterms:description
      "[CPVT CMs also displayed reduced sarcoplasmic reticulum (SR) Ca(2+) content, indicating leakage of Ca(2+) from the SR. Patch-clamp recordings of CPVT CMs revealed both delayed afterdepolarizations (DADs) during spontaneous beating and in response to adrenaline and also early afterdepolarizations (EADs) during spontaneous beating, recapitulating the changes seen in MAP and 24h-ECG recordings of patients carrying the same mutation.]. 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:22962621;
    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:NP457553.RACblkv4TX0gxNH7yEf1-TYbu10R9mLCYO26e5ntvmrqA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:32+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" .
}