@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw> .
@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:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_head {
  this: np:hasAssertion dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_assertion;
    np:hasProvenance dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_provenance;
    np:hasPublicationInfo dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_assertion a np:Assertion .
  
  dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_provenance a np:Provenance .
  
  dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_assertion {
  miriam-gene:3497 a ncit:C16612 .
  
  lld:C0270853 a ncit:C7057 .
  
  dgn-gda:DGN0e93e29f8239055eba7dbb288a5c0837 sio:SIO_000628 miriam-gene:3497, lld:C0270853;
    a sio:SIO_001121 .
}

dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_provenance {
  dgn-np:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_assertion dcterms:description
      "[Our present linkage study tested the hypothesis that DNA sequence variants associated with the gene encoding the neural cell adhesion molecule (NCAM) confer genetic susceptibility to IGE traits in 57 families ascertained through patients with either juvenile myoclonic epilepsy, juvenile or childhood absence epilepsy.]. 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:8884172;
    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:NP716978.RAdt3DBHm6rLpT-DDussBI_5mwkUm2pHVgi8p_em_u5Yw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:15+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" .
}