@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I> .
@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:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_head {
  this: np:hasAssertion dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion;
    np:hasProvenance dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_provenance;
    np:hasPublicationInfo dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion a np:Assertion .
  
  dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_provenance a np:Provenance .
  
  dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion {
  miriam-gene:6261 a ncit:C16612 .
  
  lld:C0009917 a ncit:C7057 .
  
  dgn-gda:DGN8d6c129fb40d226798d198d3be3b10bd sio:SIO_000628 miriam-gene:6261, lld:C0009917;
    a sio:SIO_001121 .
}

dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_provenance {
  dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion dcterms:description
      "[The differences between the groups in the halothane and caffeine IVCT threshold concentrations and in the time course of contracture development in the ryanodine IVCT underline the hypothesis that certain mutations in the RYR1 gene could make the ryanodine receptor more sensitive to specific ligands.]. 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:12151923;
    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:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}