@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs> .
@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:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_head {
   this: np:hasAssertion dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_assertion ;
    np:hasProvenance dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_provenance ;
    np:hasPublicationInfo dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_assertion a np:Assertion .
  dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_provenance a np:Provenance .
  dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_assertion {
   miriam-gene:1029 a ncit:C16612 .
  lld:C0086692 a ncit:C7057 .
  dgn-gda:DGN2cfb370b645f03e8354f834167cdb9f0 sio:SIO_000628 miriam-gene:1029 , lld:C0086692 ;
    a sio:SIO_001121 .
}
dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_provenance {
   dgn-np:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_assertion dcterms:description "[Promoter hypermethylation of P16, TESH, RASSF1A and RARB2 genes was noted not only in 10, 7, 19 and 13 cases of malignant tumors, but also it was detected in 7, 11, 23 and 8 cases of benign tumors, respectively, limiting its diagnostic usefulness.]. 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:20535589 ;
    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:NP766872.RAGb3Df_TEoh_xYjiI5zBaEKQfrXrj_mI4ETNs_l5cvLs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:44+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" .
}