@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8> .
@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:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_head {
  this: np:hasAssertion dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_assertion;
    np:hasProvenance dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_provenance;
    np:hasPublicationInfo dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_assertion a np:Assertion .
  
  dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_provenance a np:Provenance .
  
  dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_assertion {
  miriam-gene:89832 a ncit:C16612 .
  
  lld:C0270850 a ncit:C7057 .
  
  dgn-gda:DGNdb936ae75c002c4059010cab1a220238 sio:SIO_000628 miriam-gene:89832, lld:C0270850;
    a sio:SIO_001121 .
}

dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_provenance {
  dgn-np:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_assertion dcterms:description
      "[The aim of this work was to further evaluate the putative aetiological role of CHRNA7 in JME within the 34 families originally described, and to assess the contribution of this locus to a broader phenotype of idiopathic generalised epilepsy (IGE).]. 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:12049804;
    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:NP791293.RAsG4OKNDX9FH6HR2l_mbgmk2wuzS3I70LZS2iPc_zJH8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:05+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" .
}