@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw> .
@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:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_head {
  this: np:hasAssertion dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_assertion;
    np:hasProvenance dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_provenance;
    np:hasPublicationInfo dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_assertion a np:Assertion .
  
  dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_provenance a np:Provenance .
  
  dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_assertion {
  miriam-gene:407034 a ncit:C16612 .
  
  lld:C0011570 a ncit:C7057 .
  
  dgn-gda:DGN32742949342afaea9a94fbc854c246cb sio:SIO_000628 miriam-gene:407034, lld:C0011570;
    a sio:SIO_001122 .
}

dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_provenance {
  dgn-np:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_assertion dcterms:description
      "[To our knowledge, this is the first evidence to suggest that miRNA polymorphisms may play an important role in MDD susceptibility. These findings also imply that certain miRNAs may be involved in the etiology of MDD.]. 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:20579744;
    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:NP84778.RAiIpp9WRc3rD3DgS9afEeZhTSCBMB-McNrFaIb1pIbrw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}