@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8> .
@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:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_head {
  this: np:hasAssertion dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_assertion;
    np:hasProvenance dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_provenance;
    np:hasPublicationInfo dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_assertion a np:Assertion .
  
  dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_provenance a np:Provenance .
  
  dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_assertion {
  miriam-gene:283120 a ncit:C16612 .
  
  lld:C0699790 a ncit:C7057 .
  
  dgn-gda:DGN313e6a3b99be9737715b6f4177b17efa sio:SIO_000628 miriam-gene:283120, lld:C0699790;
    a sio:SIO_001121 .
}

dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_provenance {
  dgn-np:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_assertion dcterms:description
      "[Loss of methylation imprinting of H19 is linked to hypomethylation of the paternal allele in human bladder cancer, unlike the situation in Wilms' tumor and colon cancer where the maternal allele becomes hypermethylated.]. 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:11726548;
    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:NP265452.RAWTPbAJSS1uk3DJDOtEu-Fe3SYWEFrTKLLPwc5tz3ik8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}