@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo> .
@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:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_head {
  this: np:hasAssertion dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_assertion;
    np:hasProvenance dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_provenance;
    np:hasPublicationInfo dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_assertion a np:Assertion .
  
  dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_provenance a np:Provenance .
  
  dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_assertion {
  miriam-gene:89832 a ncit:C16612 .
  
  lld:C1510586 a ncit:C7057 .
  
  dgn-gda:DGNb57df1f8a16816b45e704c8c2a21f711 sio:SIO_000628 miriam-gene:89832, lld:C1510586;
    a sio:SIO_001121 .
}

dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_provenance {
  dgn-np:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_assertion dcterms:description
      "[Recurrent microdeletions of chromosome 15q13.3 are causally associated with autism spectrum disorders (ASDs), suggesting that haploinsufficiency of CHRNA7, the gene that codes for the α7 nicotinic acetylcholine receptor (α7 nAChR) subunit, is an etiological mechanism.]. 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:22094647;
    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:NP939640.RAT9A5JT5HnbvN8Kbf041s-SThNCLoEB46LVyiUd_UYVo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:51+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: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" .
}