@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E> .
@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:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_head {
  this: np:hasAssertion dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_assertion;
    np:hasProvenance dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_provenance;
    np:hasPublicationInfo dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_assertion a np:Assertion .
  
  dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_provenance a np:Provenance .
  
  dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0037286 a ncit:C7057 .
  
  dgn-gda:DGN30f584f73efd523ebebc4e56deb54c6b sio:SIO_000628 miriam-gene:4524, lld:C0037286;
    a sio:SIO_001122 .
}

dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_provenance {
  dgn-np:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_assertion dcterms:description
      "[Global hypomethylation appears to be a feature of SCC. Aberrant methylation of DNA appears related to polymorphisms of MTHFR. Such findings suggest that intervention in the form of demethylating agents or folate supplementation might be beneficial in the ]. 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:20346029;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP129950.RAb2_Xk5NfbWBtB24PzwqGVTtsVTt_5dNQmwr46oNqJ8E130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:53+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" .
}