@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc> .
@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/v3.0.0/void/> .
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_head {
  this: np:hasAssertion dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion ;
    np:hasProvenance dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_provenance ;
    np:hasPublicationInfo dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion a np:Assertion .
  dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_provenance a np:Provenance .
  dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  lld:C2930805 a ncit:C7057 .
  dgn-gda:DGN11b5a95c73e5089333567aa5caa33cd2 sio:SIO_000628 miriam-gene:6331 , lld:C2930805 ;
    a sio:SIO_001121 .
}
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_provenance {
  dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion dcterms:description "[Mutations in sodium channel alpha-subunit gene (SCN5A) result in multiple arrhythmic syndromes, including long QT3 (LQT3), Brugada syndrome (BS), an inherited cardiac conduction defect, sudden unexpected nocturnal death syndrome (SUNDS) and sudden infant death syndrome (SIDS), constituting a spectrum of disease entities termed Na+ channelopathies.]. 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:14753626 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:32+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}