@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c> .
@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:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_head {
  this: np:hasAssertion dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_assertion;
    np:hasProvenance dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_provenance;
    np:hasPublicationInfo dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_assertion a np:Assertion .
  
  dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_provenance a np:Provenance .
  
  dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_assertion {
  miriam-gene:5669 a ncit:C16612 .
  
  lld:C0019061 a ncit:C7057 .
  
  dgn-gda:DGN7acfb6924a2a698b8b86bebd42499d50 sio:SIO_000628 miriam-gene:5669, lld:C0019061;
    a sio:SIO_001121 .
}

dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_provenance {
  dgn-np:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_assertion dcterms:description
      "[Since Sp1 is an inducer of several genes in the presence of the inflammatory cytokines in EC, our results suggest that the transcriptional regulation of the Gb3S gene by Sp1 might affect the VT sensitivity of EC and HUS progression.]. 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:18757779;
    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:NP823048.RAHiyC2btgQngBzsfCFPeRCpcRipF-RfwAqoKzeym8H7c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:24+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" .
}