@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI> .
@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:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_head {
  this: np:hasAssertion dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_assertion;
    np:hasProvenance dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_provenance;
    np:hasPublicationInfo dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_assertion a np:Assertion .
  
  dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_provenance a np:Provenance .
  
  dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_assertion {
  miriam-gene:2904 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGNbe0c09d57b73a72bdf8be340e4750d41 sio:SIO_000628 miriam-gene:2904, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_provenance {
  dgn-np:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_assertion dcterms:description
      "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. 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:22833210;
    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:NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:16+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" .
}