@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg> .
@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:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_head {
   this: np:hasAssertion dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_assertion ;
    np:hasProvenance dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_provenance ;
    np:hasPublicationInfo dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_assertion a np:Assertion .
  dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_provenance a np:Provenance .
  dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_assertion {
   miriam-gene:282553 a ncit:C16612 .
  lld:C0042798 a ncit:C7057 .
  dgn-gda:DGNbaa38317a0bee8631dc5c985d59af5e7 sio:SIO_000628 miriam-gene:282553 , lld:C0042798 ;
    a sio:SIO_001121 .
}
dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_provenance {
   dgn-np:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_assertion dcterms:description "[Nucleotide changes in the AUTS2 locus, some of which affect only noncoding regions, are associated with autism and other neurological disorders, including attention deficit hyperactivity disorder, epilepsy, dyslexia, motor delay, language delay, visual impairment, microcephaly, and alcohol consumption.]. 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:23349641 ;
    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:NP181657.RAq-VloV_zgdbz0UPFduBefxIA8ZjR3Hkk33uuhny2phg130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:38+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" .
}