@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg> .
@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:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_head {
  this: np:hasAssertion dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion;
    np:hasProvenance dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_provenance;
    np:hasPublicationInfo dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion a np:Assertion .
  
  dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_provenance a np:Provenance .
  
  dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion {
  miriam-gene:3362 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN9339f18803628337d2b5e1ad845c63dd sio:SIO_000628 miriam-gene:3362, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_provenance {
  dgn-np:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_assertion dcterms:description
      "[These polymorphisms probably do not represent major genetic risk factors of AD. However, further studies including other genetic variants of the serotonergic neurotransmitter system are needed in order to elucidate their role in AD. ]. 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:11692286;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP57220.RAd8gSXgnqT_hdchOaHZMSwmeBYG5TMAfzViY2uM_FeVg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}