@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c> .
@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:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_head {
  this: np:hasAssertion dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_assertion;
    np:hasProvenance dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_provenance;
    np:hasPublicationInfo dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_assertion a np:Assertion .
  
  dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_provenance a np:Provenance .
  
  dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_assertion {
  miriam-gene:1785 a ncit:C16612 .
  
  lld:C0023976 a ncit:C7057 .
  
  dgn-gda:DGNbb95692117c690b98fc57408da0a1861 sio:SIO_000628 miriam-gene:1785, lld:C0023976;
    a sio:SIO_001121 .
}

dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_provenance {
  dgn-np:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_assertion dcterms:description
      "[The cytoskeletal protein syntrophin-alpha(1) (SNTA1) is known to interact with the cardiac sodium channel (hNa(v)1.5), and we hypothesized that SNTA1 mutations might cause phenotypic LQTS in patients with genotypically normal hNa(v)1.5 by secondarily disturbing sodium channel function.]. 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:19684871;
    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:NP757917.RACxHCUBpndejbqx2_wo83VSMY5bc8OT3_tEVDxXGaf-c130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:28+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" .
}