@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U> .
@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:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_head {
  this: np:hasAssertion dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_assertion ;
    np:hasProvenance dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_provenance ;
    np:hasPublicationInfo dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_assertion a np:Assertion .
  dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_provenance a np:Provenance .
  dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_assertion {
  miriam-gene:7436 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGN70522e2abcd31732e4877122f1f5054e sio:SIO_000628 miriam-gene:7436 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_provenance {
  dgn-np:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_assertion dcterms:description "[We examined the polymorphic CGG repeat in the 5'-untranslated region (UTR) of the reelin gene, which was recently found to be associated with autistic disorder, and the CGG repeat in the 5' UTR region of the very low density protein receptor (VLDLR) gene, which was reported to be associated with sporadic Alzheimer's disease, for allelic association with 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:12363388 ;
    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:NP900002.RAcqYO5KKPXuGj4AShMs-1iwXD3estQCMewN1pTGBNf5U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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" .
}