@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_head {
  this: np:hasAssertion dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_assertion;
    np:hasProvenance dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_provenance;
    np:hasPublicationInfo dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_assertion a np:Assertion .
  
  dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_provenance a np:Provenance .
  
  dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_assertion {
  miriam-gene:10618 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGNf7573f4c6f9e4826bd6b1522eb0c849b sio:SIO_000628 miriam-gene:10618, lld:C0525045;
    a sio:SIO_001121 .
}

dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_provenance {
  dgn-np:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_assertion dcterms:description
      "[Taken together, these analyses do not provide support for the hypothesis that common genetic variation in TGOLN2 contributes significantly to the risk for attempted suicide in subjects with major mood disorders.]. 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:20468057;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP848873.RAmBERP2A-wtUYKrs8zaU970pwdPeVw3HKyZ4k4OsyI5Q130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:15+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}