@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs> .
@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:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_head {
   this: np:hasAssertion dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_assertion ;
    np:hasProvenance dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_provenance ;
    np:hasPublicationInfo dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_assertion a np:Assertion .
  dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_provenance a np:Provenance .
  dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_assertion {
   miriam-gene:6584 a ncit:C16612 .
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dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_provenance {
   dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_assertion dcterms:description "[The study of SCD has focused on several major themes: progress in understanding the causes and treatments of genetic cardiovascular diseases, improved management of patients with congenital heart disease with SCD risk, treatment strategies for SCD risk reduction in patients with cardiomyopathies, and defining guidelines for athletic preparticipation screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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dgn-np:NP618064.RAANlGjMoCDGcgqH0YjrOFwePUX7t9xrQIRuf_UU6gdRs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:13+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}