@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI> .
@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:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_head {
  this: np:hasAssertion dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_assertion;
    np:hasProvenance dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_provenance;
    np:hasPublicationInfo dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_assertion a np:Assertion .
  
  dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_provenance a np:Provenance .
  
  dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_assertion {
  miriam-gene:1789 a ncit:C16612 .
  
  lld:C0699791 a ncit:C7057 .
  
  dgn-gda:DGN7b2b05d44f864648f04faaba2e7596dc sio:SIO_000628 miriam-gene:1789, lld:C0699791;
    a sio:SIO_001121 .
}

dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_provenance {
  dgn-np:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_assertion dcterms:description
      "[The aim of this study was to detect the expression pattern of DNA methyltransferase 3B (DNMT3B) variants in primary gastric cancer (GC) and to explore the clinical significance of DNMT3B variants in gastric carcinogenesis.]. 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:20127025;
    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:NP243891.RAwLBsc4kRsnXmdiftio5r9wCtr88XZhz7UOUIpBBG7lI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:16+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" .
}