@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM> .
@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:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_head {
  this: np:hasAssertion dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_assertion;
    np:hasProvenance dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_provenance;
    np:hasPublicationInfo dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_assertion a np:Assertion .
  
  dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_provenance a np:Provenance .
  
  dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_assertion {
  miriam-gene:339488 a ncit:C16612 .
  
  lld:C0001430 a ncit:C7057 .
  
  dgn-gda:DGN220131e74441a7912b808e0820b6dbb0 sio:SIO_000628 miriam-gene:339488, lld:C0001430;
    a sio:SIO_001121 .
}

dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_provenance {
  dgn-np:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_assertion dcterms:description
      "[In a larger independent cohort of adenomas, for genes in which hypermethylation had been validated, different frequencies of hypermethylation were apparent, where the KIAA1822 (HHIPL1) and TFAP2E genes were hypermethylated in 12 of 13 NF adenomas whereas the COL1A2 gene showed an increase in two of 13 adenomas.]. 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:23045325;
    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:NP889368.RAGrdZKfM3N0tLmD14nUlOZ-CcZ77X74-cq9D8s7sDhmM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:06+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" .
}