@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI> .
@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:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_head {
  this: np:hasAssertion dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_assertion;
    np:hasProvenance dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_provenance;
    np:hasPublicationInfo dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_assertion a np:Assertion .
  
  dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_provenance a np:Provenance .
  
  dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_assertion {
  miriam-gene:1012 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGNacd2274843f77a0c940422bc87bdace4 sio:SIO_000628 miriam-gene:1012, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_provenance {
  dgn-np:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_assertion dcterms:description
      "[Thus, 40 Wilms' tumours and up to 49 adult RCC were analysed by methylation-specific PCR for promoter methylation at CASP8, CDH1, CDH13, DAPK, MGMT, NORE1A, p14ARF and RARB2 in primary Wilms' tumours and CASP8, CDH1, CDH13, CRBP1, DAPK, MGMT, MT1G, NORE1A, p16INK4a, SDHB and RARB2 in primary RCC.]. 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:14555992;
    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:NP157712.RAt0V_-Z2MjVsoG-1nfQzi8c2orqDq1L3-qZsNt29PvrI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}