@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0> .
@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:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_head {
  this: np:hasAssertion dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_assertion ;
    np:hasProvenance dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_provenance ;
    np:hasPublicationInfo dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_assertion a np:Assertion .
  dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_provenance a np:Provenance .
  dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_assertion {
  miriam-gene:80199 a ncit:C16612 .
  lld:C0080174 a ncit:C7057 .
  dgn-gda:DGNcd33040e0969aa397b01eab6f8d67e13 sio:SIO_000628 miriam-gene:80199 , lld:C0080174 ;
    a sio:SIO_001121 .
}
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_provenance {
  dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_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:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:08+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" .
}