@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ> .
@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:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_head {
  this: np:hasAssertion dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_assertion;
    np:hasProvenance dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_provenance;
    np:hasPublicationInfo dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_assertion a np:Assertion .
  
  dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_provenance a np:Provenance .
  
  dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_assertion {
  miriam-gene:2020 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGNe2eddb36a6b5982fae47a4f8f8e7e8b3 sio:SIO_000628 miriam-gene:2020, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_provenance {
  dgn-np:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_assertion dcterms:description
      "[Future studies investigating EN2 should consider how the association of variants in this gene with autism could be influenced by differences in phenotype and possible interactions with genotypes at other autism candidate genes.]. 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:17948868;
    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:NP165110.RA1swvgRrkL5E0Rf1bSiQbMF2fj_golyY7rR3N_clAQfQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}