@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE> .
@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:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_head {
  this: np:hasAssertion dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_assertion ;
    np:hasProvenance dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_provenance ;
    np:hasPublicationInfo dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_assertion a np:Assertion .
  dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_provenance a np:Provenance .
  dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_assertion {
  miriam-gene:846 a ncit:C16612 .
  lld:C0700095 a ncit:C7057 .
  dgn-gda:DGN306222ba1913fc09036edfc879d66cd3 sio:SIO_000628 miriam-gene:846 , lld:C0700095 ;
    a sio:SIO_001121 .
}
dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_provenance {
  dgn-np:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_assertion dcterms:description "[These data would support the hypothesis that epigenetic silencing of the CaSR gene is neither an in vitro artefact in neuroblastoma cell lines nor an irrelevant, secondary event in primary NTs, but a significant mechanism for neuroblastoma survival.]. 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:23108190 ;
    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:NP283065.RAcekmCTNH1Nf3Nr_7YHMgjxWe-NlphgTJAvHLXwenqGE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:21+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" .
}