@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c> .
@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:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_head {
   this: np:hasAssertion dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_assertion ;
    np:hasProvenance dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_provenance ;
    np:hasPublicationInfo dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_assertion a np:Assertion .
  dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_provenance a np:Provenance .
  dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_assertion {
   miriam-gene:26053 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGNaa3b8678927027370c97aff1e4a3776f sio:SIO_000628 miriam-gene:26053 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_provenance {
   dgn-np:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_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:NP486466.RAmpPjkMw-IByYZu8GC1bt1wNwDynUKvCK4FuVfxz6T3c130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:51+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" .
}