@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo> .
@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:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_head {
  this: np:hasAssertion dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_assertion ;
    np:hasProvenance dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_provenance ;
    np:hasPublicationInfo dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_assertion a np:Assertion .
  dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_provenance a np:Provenance .
  dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_assertion {
  miriam-gene:80199 a ncit:C16612 .
  lld:C0270850 a ncit:C7057 .
  dgn-gda:DGNb05ad3fa2c32a8d879841e45ebdf730a sio:SIO_000628 miriam-gene:80199 , lld:C0270850 ;
    a sio:SIO_001121 .
}
dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_provenance {
  dgn-np:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_assertion dcterms:description "[Spina bifida occulta, defined as a nonsymptomatic nonfusion of vertebral arches, has been suggested to be genetically determined, with an increased prevalence in patients with primary generalized epilepsy, and that the presence of this trait in fetal development can be enhanced pharmacologically to produce NTD such as meningomyelocele.]. 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:8156953 ;
    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:NP452622.RA6CJLZfgXYHR7hW7348o9bh5dKmNvtKrXuGNg1TeC6qo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:30+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" .
}