@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw> .
@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:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_head {
   this: np:hasAssertion dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_assertion ;
    np:hasProvenance dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_provenance ;
    np:hasPublicationInfo dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_assertion a np:Assertion .
  dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_provenance a np:Provenance .
  dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_assertion {
   miriam-gene:11186 a ncit:C16612 .
  lld:C0040136 a ncit:C7057 .
  dgn-gda:DGNa18128ce8322eaa421c2aa0ac15f5bf5 sio:SIO_000628 miriam-gene:11186 , lld:C0040136 ;
    a sio:SIO_001121 .
}
dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_provenance {
   dgn-np:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_assertion dcterms:description "[The mean levels of hypermethylation of P16, TSHR and RASSF1A genes were significantly higher in malignant papillary thyroid tumors compared to benign tumors and by choosing the appropriate cutoff for each gene, we could distinguish 9, 9 and 8 PTCs from 25 cases by P16, RASSF1A and TSHR methylation analysis, respectively.]. 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:NP375947.RAdrCN8P54Vja18kOMGB7340NoEYRTprZ9_YACIXwcEAw130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:40+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> ;
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}