@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0> .
@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:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_head {
  this: np:hasAssertion dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion;
    np:hasProvenance dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_provenance;
    np:hasPublicationInfo dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion a np:Assertion .
  
  dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_provenance a np:Provenance .
  
  dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion {
  miriam-gene:2914 a ncit:C16612 .
  
  lld:C0014553 a ncit:C7057 .
  
  dgn-gda:DGN3b70a82a751ccc85966d2bf3ef96cfbb sio:SIO_000628 miriam-gene:2914, lld:C0014553;
    a sio:SIO_001122 .
}

dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_provenance {
  dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion dcterms:description
      "[Association analysis was carried out for 17 single nucleotide polymorphisms (SNPs) covering the genomic GRM4 sequence for all IGE patients as well as for two common IGE subsyndromes Juvenile Myoclonic Epilepsy (JME, n=215) and Childhood Absence Epilepsy (CAE, n=175).]. 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:20338729;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:03+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" .
}