@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4> .
@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:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_head {
  this: np:hasAssertion dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_assertion;
    np:hasProvenance dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_provenance;
    np:hasPublicationInfo dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_assertion a np:Assertion .
  
  dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_provenance a np:Provenance .
  
  dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_assertion {
  miriam-gene:199699 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN83ed15d6738309d8a343769f1a5dbf33 sio:SIO_000628 miriam-gene:199699, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_provenance {
  dgn-np:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_assertion dcterms:description
      "[Analysis of functional modules revealed the possible regulatory roles of SP1 and CXCL12 in the pathogenesis of cardiovascular disease (CVD) and modulation of their activities may be considered as potential therapeutic tools.]. 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:21559538;
    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:NP204418.RARYYZK9a_Rgp-x9Hl_beaSuShS8AGZ2N0vbUN4y1Vie4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:52+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" .
}