@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U> .
@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:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_head {
  this: np:hasAssertion dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_assertion;
    np:hasProvenance dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_provenance;
    np:hasPublicationInfo dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_assertion a np:Assertion .
  
  dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_provenance a np:Provenance .
  
  dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  
  lld:C0268446 a ncit:C7057 .
  
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    a sio:SIO_001122 .
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dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_provenance {
  dgn-np:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_assertion dcterms:description
      "[It is suggested that the SNP distribution of SCN5A gene varies within different nationalities. These data will be of use for genetic association studies of acquired arrythmias and investigation of sensitivity to drug therapy.]. 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:14985827;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52125.RA4kE19NAKpmqHKTrhzgHcRnzq-IQbGUFzzhj6MwUng5U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}