@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M> .
@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:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_head {
  this: np:hasAssertion dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_assertion;
    np:hasProvenance dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_provenance;
    np:hasPublicationInfo dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_assertion a np:Assertion .
  
  dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_provenance a np:Provenance .
  
  dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNb3fad340022b98d3c7407e05bda036fc sio:SIO_000628 miriam-gene:3630, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_provenance {
  dgn-np:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_assertion dcterms:description
      "[Claiming that the result of genotyping predicts optimal treatment in certain epilepsies is equivalent to stating that genotyping for diabetes has become available and that, based on this breakthrough, insulin can now be selected as the treatment of choice in those who test positive.]. 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:19087113;
    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:NP709584.RAjVi3it5dyA1nxeRvFoMurFSOuof2w7R66i5e1NVHH8M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:06+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" .
}