@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g> .
@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:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_head {
  this: np:hasAssertion dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_assertion;
    np:hasProvenance dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_provenance;
    np:hasPublicationInfo dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_assertion a np:Assertion .
  
  dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_provenance a np:Provenance .
  
  dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_assertion {
  miriam-gene:6262 a ncit:C16612 .
  
  lld:C0002895 a ncit:C7057 .
  
  dgn-gda:DGN80576bfd1cdcdceade80f491427f33d4 sio:SIO_000628 miriam-gene:6262, lld:C0002895;
    a sio:SIO_001121 .
}

dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_provenance {
  dgn-np:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_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:NP438796.RA4IfiqT5CT_Q8YE8LNwVw8ts1Feq2i5GG7asnDjLOw5g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:19+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" .
}