@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI> .
@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:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_head {
  this: np:hasAssertion dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion;
    np:hasProvenance dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_provenance;
    np:hasPublicationInfo dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion a np:Assertion .
  
  dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_provenance a np:Provenance .
  
  dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion {
  miriam-gene:2903 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGNe0f922209650cd4fa2cec945c61f15ee sio:SIO_000628 miriam-gene:2903, lld:C1263846;
    a sio:SIO_001121 .
}

dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_provenance {
  dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion dcterms:description
      "[Our data suggest that genetic variation in GRIN2A may confer increased risk for ADHD and that this, at least in part, might be responsible for the linkage result on 16p reported by Smalley et al.]. 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:14966475;
    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:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:53+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" .
}