@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_head {
  this: np:hasAssertion dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_assertion;
    np:hasProvenance dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_provenance;
    np:hasPublicationInfo dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_assertion a np:Assertion .
  
  dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_provenance a np:Provenance .
  
  dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_assertion {
  miriam-gene:6261 a ncit:C16612 .
  
  lld:C0024591 a ncit:C7057 .
  
  dgn-gda:DGN65b758947ba3f6694056a7a4717b7482 sio:SIO_000628 miriam-gene:6261, lld:C0024591;
    a sio:SIO_001121 .
}

dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_provenance {
  dgn-np:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_assertion dcterms:description
      "[Our study contributes to the genetic aetiology of MH in Sweden, but also raises questions about the involvement of genes other than RYR1 since nearly half of the probands did not show any sequence variants in the total coding region of the RYR1.]. 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:19346234;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP730600.RAIz7o-5tQm9BFNbHfkfpdh7OFsK37xpww2ErARFYtSNs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:16+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}