@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI> .
@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:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_head {
  this: np:hasAssertion dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_assertion;
    np:hasProvenance dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_provenance;
    np:hasPublicationInfo dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_assertion a np:Assertion .
  
  dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_provenance a np:Provenance .
  
  dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C3698186 a ncit:C7057 .
  
  dgn-gda:DGN3799fc8fa96b441d0bc5208adf867f49 sio:SIO_000628 miriam-gene:3757, lld:C3698186;
    a sio:SIO_001121 .
}

dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_provenance {
  dgn-np:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_assertion dcterms:description
      "[Adhering to the recommendations of including molecular diagnostics of cardiac channelopathies in SUD investigation, the Molecular Genetics Laboratory of the New York City (NYC) Office of Chief Medical Examiner (OCME) has been routinely testing for six major channelopathy genes (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, and RyR2) since 2008.]. 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:24631775;
    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:NP1164141.RAm5S7N56Ct9isrn2eMgk1vYOGEtNZJH-QTALP5tSTwtI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:33+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" .
}