@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4> .
@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:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_head {
   this: np:hasAssertion dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_assertion ;
    np:hasProvenance dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_provenance ;
    np:hasPublicationInfo dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_assertion a np:Assertion .
  dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_provenance a np:Provenance .
  dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_assertion {
   miriam-gene:282553 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGN76511c6b21f70f3cfffb2389038e93c3 sio:SIO_000628 miriam-gene:282553 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_provenance {
   dgn-np:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_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:NP340155.RACtBi02rj50QNlXsPWe5xL9Pu0ihliFMA5ien1aPj2W4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:20+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" .
}