@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM> .
@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:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_head {
  this: np:hasAssertion dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_assertion;
    np:hasProvenance dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_provenance;
    np:hasPublicationInfo dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_assertion a np:Assertion .
  
  dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_provenance a np:Provenance .
  
  dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_assertion {
  miriam-gene:424 a ncit:C16612 .
  
  lld:C0002895 a ncit:C7057 .
  
  dgn-gda:DGNd56416f87ca0aea3aa135740c4d2ad75 sio:SIO_000628 miriam-gene:424, lld:C0002895;
    a sio:SIO_001121 .
}

dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_provenance {
  dgn-np:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_assertion dcterms:description
      "[The cardiac ryanodine receptor (RyR2), the major calcium release channel on the sarcoplasmic reticulum (SR) in cardiomyocytes, has recently been shown to be involved in at least two forms of sudden cardiac death (SCD): (1) Catecholaminergic polymorphic ventricular tachycardia (CPVT) or familial polymorphic VT (FPVT); and (2) Arrhythmogenic right ventricular dysplasia type 2 (ARVD2).]. 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:11807805;
    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:NP757249.RAIclctCDIrW5AkncNvCF8VqAWtFq4qwgDCQAii7JnVlM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:38+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" .
}