@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68> .
@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:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_head {
  this: np:hasAssertion dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_assertion;
    np:hasProvenance dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_provenance;
    np:hasPublicationInfo dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_assertion a np:Assertion .
  
  dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_provenance a np:Provenance .
  
  dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_assertion {
  miriam-gene:779 a ncit:C16612 .
  
  lld:C0751951 a ncit:C7057 .
  
  dgn-gda:DGNc557c7c23456413f3fca062eb70c422e sio:SIO_000628 miriam-gene:779, lld:C0751951;
    a sio:SIO_001121 .
}

dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_provenance {
  dgn-np:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_assertion dcterms:description
      "[It provides a time line over the past half century of the highlights of research on malignant hyperthermia (MH), central core disease (CCD) and catecholaminergic polymorphic ventricular tachycardia (CPVT), that resulted in the identification of the ryanodine receptor (RYR), calsequestrin (CASQ) and dihydropyridine receptor (CACNA1S) genes as sites of disease-causing mutations.]. 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:21118704;
    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:NP868158.RAQqoltoCWsc6RF7Bh84IezIbhT_QZR_2m9woNqLOfj68130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:50+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" .
}