@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs> .
@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:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_head {
  this: np:hasAssertion dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_assertion;
    np:hasProvenance dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_provenance;
    np:hasPublicationInfo dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_assertion a np:Assertion .
  
  dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_provenance a np:Provenance .
  
  dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_assertion {
  miriam-gene:1140 a ncit:C16612 .
  
  lld:C0751885 a ncit:C7057 .
  
  dgn-gda:DGN34e11d247391c842cd1787b8ba49d207 sio:SIO_000628 miriam-gene:1140, lld:C0751885;
    a sio:SIO_001121 .
}

dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_provenance {
  dgn-np:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_assertion dcterms:description
      "[Because levels of quinidine sulfate attainable in clinical practice shorten the opening episodes of genetically engineered mutant SCCMS receptors in vitro, we tested the notion that the drug can be of benefit in SCCMS.]. 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:9546329;
    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:NP784603.RADAXAktcK_UTOf7T5moAMhdaQmW3PSyrnBHgyoCVPNIs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:55+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" .
}