@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k> .
@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:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_head {
  this: np:hasAssertion dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion;
    np:hasProvenance dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_provenance;
    np:hasPublicationInfo dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion a np:Assertion .
  
  dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_provenance a np:Provenance .
  
  dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion {
  miriam-gene:11331 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGN10aa6555cc9df250f4ca9a1695b3ad9c sio:SIO_000628 miriam-gene:11331, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_provenance {
  dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion dcterms:description
      "[Given the recent findings regarding the association between alexithymia and Autism Spectrum Disorder (ASD) and the accumulating evidence for the presence of the Broader Autism Phenotype (BAP) in relatives of individuals with ASD, we further explored the construct of alexithymia in parents of children with ASD as a potential part of the BAP.]. 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:18473159;
    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:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:01+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" .
}