@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c> .
@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:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_head {
  this: np:hasAssertion dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_assertion;
    np:hasProvenance dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_provenance;
    np:hasPublicationInfo dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_assertion a np:Assertion .
  
  dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_provenance a np:Provenance .
  
  dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_assertion {
  miriam-gene:6319 a ncit:C16612 .
  
  lld:C0012833 a ncit:C7057 .
  
  dgn-gda:DGN5736ae013da1a5777e45768676fc2c6e sio:SIO_000628 miriam-gene:6319, lld:C0012833;
    a sio:SIO_001121 .
}

dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_provenance {
  dgn-np:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_assertion dcterms:description
      "[Although SCD may be the first presentation of arrhythmic syndromes, patients may present to the general physician with symptoms of palpitations or hemodynamic compromise, including dizziness, seizure, or syncope, particularly following exertion.]. 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:23651009;
    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:NP541341.RA14f2cFP4NOB9y3JHfBMRg0Th7W3hXcuT25rWbFdKW4c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:26+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" .
}