@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js> .
@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:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_head {
  this: np:hasAssertion dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_assertion ;
    np:hasProvenance dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_provenance ;
    np:hasPublicationInfo dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_assertion a np:Assertion .
  dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_provenance a np:Provenance .
  dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_assertion {
  miriam-gene:730249 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
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dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_provenance {
  dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_assertion dcterms:description "[In addition, although it is plausible that genetic variation related to inflammation and serotonin may be associated with both depression and CAD, genetic variation related to inflammation has been primary examined in relation to CAD, whereas genetic variation in the serotonin system has been primarily examined in relation to depression.]. 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:16554382 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP1011246.RAA4LGhoXQ4ryuwB-lnhHFEg1i4XmfthapekLRFyyR7js130_publicationInfo {
  this: dcterms:created "2015-08-25T14:48:07+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}