@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns> .
@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:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_head {
  this: np:hasAssertion dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_assertion;
    np:hasProvenance dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_provenance;
    np:hasPublicationInfo dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_assertion a np:Assertion .
  
  dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_provenance a np:Provenance .
  
  dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C0279626 a ncit:C7057 .
  
  dgn-gda:DGN6485a8cdf5b0687b15b6ebba0ec2b7ec sio:SIO_000628 miriam-gene:4292, lld:C0279626;
    a sio:SIO_001121 .
}

dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_provenance {
  dgn-np:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_assertion dcterms:description
      "[Our results suggest that hypermethylation of key genes, such as p16(INK4a), p14(ARF) and hMLH1, may be used in combination with other molecular changes, such as p53 mutation, in the development of biomarkers for predicting the risk for ESCC.]. 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:12376481;
    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:NP558395.RAM8Q0Rtp6YNiEZThMsL5BKPnpC5v-PhrkBImYTBBu3Ns130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:12+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" .
}