@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g> .
@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:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_head {
  this: np:hasAssertion dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion;
    np:hasProvenance dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_provenance;
    np:hasPublicationInfo dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion a np:Assertion .
  
  dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_provenance a np:Provenance .
  
  dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion {
  miriam-gene:3784 a ncit:C16612 .
  
  lld:C1141890 a ncit:C7057 .
  
  dgn-gda:DGN0aa5a78c55ce51d8a00d7e295cca2e0d sio:SIO_000628 miriam-gene:3784, lld:C1141890;
    a sio:SIO_001121 .
}

dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_provenance {
  dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion dcterms:description
      "[The most prevalent LQT1 form of inherited long QT syndrome is caused by mutations of the KCNQ1 gene resulting repolarizing I(Ks) potassium current to decrease and the QT interval to prolong.]. 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:17023080;
    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:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:05+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" .
}