@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4> .
@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:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_head {
  this: np:hasAssertion dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_assertion ;
    np:hasProvenance dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_provenance ;
    np:hasPublicationInfo dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_assertion a np:Assertion .
  dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_provenance a np:Provenance .
  dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_assertion {
  miriam-gene:55749 a ncit:C16612 .
  lld:C0812393 a ncit:C7057 .
  dgn-gda:DGNdef66079508c188ba43fc11261ec39b3 sio:SIO_000628 miriam-gene:55749 , lld:C0812393 ;
    a sio:SIO_001121 .
}
dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_provenance {
  dgn-np:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_assertion dcterms:description "[We used a family study approach to examine validity and found that both the DIS and IDD cases of depression were two to three times more frequent in the relatives of depressed patients than the relatives of schizophrenics and controls.]. 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:3395202 ;
    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:NP715898.RAj2FnC_nFAxPEaq4M0p1k5FXpWJl55NW-KfHdG3BfnW4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:15+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}