@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g> .
@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:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_head {
  this: np:hasAssertion dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_assertion;
    np:hasProvenance dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_provenance;
    np:hasPublicationInfo dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_assertion a np:Assertion .
  
  dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_provenance a np:Provenance .
  
  dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_assertion {
  miriam-gene:9378 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGNda5d13bbb954116b0ac669891645126b sio:SIO_000628 miriam-gene:9378, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_provenance {
  dgn-np:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_assertion dcterms:description
      "[Since this represents one of the core symptom domains affected in autism spectrum disorders and schizophrenia in humans, our findings suggest that deletions within NRXN1 found in patients may be responsible for the impairments seen in social behaviours, and that the Nrxn1α KO mice are a useful model of human neurodevelopmental disorder.]. 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:23840597;
    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:NP154521.RAf83nQeEptNVxXybLTdCVh2B3auQFmSHG1cWqd8QWe5g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}