@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_head {
   this: np:hasAssertion dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_assertion ;
    np:hasProvenance dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_provenance ;
    np:hasPublicationInfo dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_assertion a np:Assertion .
  dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_provenance a np:Provenance .
  dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_assertion {
   miriam-gene:91752 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGNc3cadf72a0b67663004cd7699ad4e3d6 sio:SIO_000628 miriam-gene:91752 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_provenance {
   dgn-np:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_assertion dcterms:description "[For example, variation at ZNF804A is associated with risk of both bipolar disorder and schizophrenia, and some rare CNVs are associated with risk of autism and epilepsy as well as schizophrenia.]. 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:19329560 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP729091.RAI2OeMzeYdbJALZ2TBh8XSZhI8aCP6BfZBndwswBpaPk130_publicationInfo {
   this: dcterms:created "2016-05-13T12:47:15+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}