@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI> .
@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:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_head {
  this: np:hasAssertion dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_assertion;
    np:hasProvenance dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_provenance;
    np:hasPublicationInfo dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_assertion a np:Assertion .
  
  dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_provenance a np:Provenance .
  
  dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_assertion {
  miriam-gene:11258 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGN8a8998729d1ea0c5656affe3ec293409 sio:SIO_000628 miriam-gene:11258, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_provenance {
  dgn-np:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_assertion dcterms:description
      "[This analysis not only has confirmed the presence of several known autism risk regions but has also revealed additional previously unidentified loci, including 2q37, 5p15, 11q25, 16q22.3, 17p11.2, 18q21.1, 18q23, 22q11.2, 22q13.3 and Xp22.2-p22.3.]. 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:16205736;
    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:NP793614.RAs2fdsta8zaZiWp7Yj5qXmChTnHZVEZgBxspa3oDennI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:07+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" .
}