@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk> .
@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:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_head {
   this: np:hasAssertion dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_assertion ;
    np:hasProvenance dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_provenance ;
    np:hasPublicationInfo dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_assertion a np:Assertion .
  dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_provenance a np:Provenance .
  dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_assertion {
   miriam-gene:6331 a ncit:C16612 .
  lld:C0007193 a ncit:C7057 .
  dgn-gda:DGNffa8a32953bb56c20ee35024be37ecd1 sio:SIO_000628 miriam-gene:6331 , lld:C0007193 ;
    a sio:SIO_001121 .
}
dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_provenance {
   dgn-np:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_assertion dcterms:description "[Over the past years, hundreds of mutations in SCN5A, the human gene coding for NaV1.5, have been linked to many cardiac electrical disorders, including the congenital and acquired long QT syndrome, Brugada syndrome, conduction slowing, sick sinus syndrome, atrial fibrillation, and dilated cardiomyopathy.]. 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:23123192 ;
    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:NP765199.RAWWQVrHPOMDonpoJ4sh1y0dmhgX850UFryH4FoR9hqAk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:43+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" .
}