@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc> .
@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/v3.0.0/void/> .

dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_head {
  this: np:hasAssertion dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_assertion;
    np:hasProvenance dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_provenance;
    np:hasPublicationInfo dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_assertion a np:Assertion .
  
  dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_provenance a np:Provenance .
  
  dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C0018817 a ncit:C7057 .
  
  dgn-gda:DGN534f8aabb7d2b8c5ddfb533ab746ce8b sio:SIO_000628 miriam-gene:2477, lld:C0018817;
    a sio:SIO_001121 .
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dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_provenance {
  dgn-np:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_assertion dcterms:description
      "[Here, we review the existing data on the phenotypes of mice carrying mutations in genes associated with ASD including neuroligin, neurexin and Shank mutant mice as well as the Fmr1, Mecp2, Ube3a, Nf1, Pten and Tsc1/Tsc2 mutant mice.]. 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:21328568;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP412453.RA0zwIkRyIkqLx64iuszQjQvbfdGODURT-BExpJ21owpc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:40+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}