@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q> .
@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:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_head {
  this: np:hasAssertion dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion ;
    np:hasProvenance dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion a np:Assertion .
  dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_provenance a np:Provenance .
  dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion {
  miriam-gene:1268 a ncit:C16612 .
  lld:C0030567 a ncit:C7057 .
  dgn-gda:DGN47aecc1f2eeee000c788ce994ce1e253 sio:SIO_000628 miriam-gene:1268 , lld:C0030567 ;
    a sio:SIO_001121 .
}
dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_provenance {
  dgn-np:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_assertion dcterms:description "[The cloning of the human cannabinoid receptor (CNR1) gene facilitates molecular genetic studies in disorders like Gilles de la Tourette syndrome (GTS), obsessive compulsive disorder (OCD), Parkinsons disease, Alzheimers disease or other neuro psychiatric or neurological diseases, which may be predisposed or influenced by mutations or variants in the CNR1 gene.]. 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:10441206 ;
    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:NP825236.RAHmXY_VTxhG2gAMwq1GzBz90ljOMzX2zcvL8HMX9IT9Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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" .
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}