@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE> .
@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:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_head {
  this: np:hasAssertion dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion;
    np:hasProvenance dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_provenance;
    np:hasPublicationInfo dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion a np:Assertion .
  
  dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_provenance a np:Provenance .
  
  dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  
  lld:C0023976 a ncit:C7057 .
  
  dgn-gda:DGN4108455b96bf4e48a90b3f40859f0f60 sio:SIO_000628 miriam-gene:6331, lld:C0023976;
    a sio:SIO_001121 .
}

dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_provenance {
  dgn-np:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_assertion dcterms:description
      "[In the last few years, a very active line of research took place after the first identification of SCN5A mutations associated with an inherited form of cardiac arrhythmias and sudden death, the LQT3 variant of the long QT syndrome.]. 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:12747584;
    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:NP394301.RAlcMzDXukuECY7OHjgR9Dtt8bOKWMwmt3FimhH6B60OE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:44+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" .
}