@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk> .
@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:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_head {
  this: np:hasAssertion dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_assertion;
    np:hasProvenance dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_provenance;
    np:hasPublicationInfo dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_assertion a np:Assertion .
  
  dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_provenance a np:Provenance .
  
  dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_assertion {
  miriam-gene:2904 a ncit:C16612 .
  
  lld:C0279626 a ncit:C7057 .
  
  dgn-gda:DGNe65e49834c4ee5563a756a5e7072231b sio:SIO_000628 miriam-gene:2904, lld:C0279626;
    a sio:SIO_001121 .
}

dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_provenance {
  dgn-np:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_assertion dcterms:description
      "[To investigate whether the promoter methylation pattern in N-methyl-d-aspartate receptor 2B (NMDAR2B) is correlated with clinical features of human esophageal squamous cell carcinoma (ESCC), the methylation status of the gene was examined at three different sites (P1, P2, and P3) where two CpG islands reside within 1 kb upstream of the transcription start site.]. 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:18006766;
    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:NP765115.RAjCQnFdiqSCz_VbPX6elrw09LAdQuv4wYHf-vMOTOmpk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:43+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" .
}