@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g> .
@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/v4.0.0/void/> .

dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_head {
  this: np:hasAssertion dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_assertion;
    np:hasProvenance dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_provenance;
    np:hasPublicationInfo dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_assertion a np:Assertion .
  
  dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_provenance a np:Provenance .
  
  dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_assertion {
  miriam-gene:635 a ncit:C16612 .
  
  lld:C0278996 a ncit:C7057 .
  
  dgn-gda:DGNaec7f909f2f2760ef10d9a1c6085857b sio:SIO_000628 miriam-gene:635, lld:C0278996;
    a sio:SIO_001122 .
}

dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_provenance {
  dgn-np:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_assertion dcterms:description
      "[We conducted a case-control study (265 HNSCC cases and 466 non-cancer controls) to investigate associations of MTHFR C677T and A1298C, MTR A2756G, MTRR A66G, RFC1 A80G, MTHFD1 G1958A, CBS 844ins68, TC2 C776G and A67G, SHMT C1420T and BHMT G742A polymorphisms with HNSCC risk.]. 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:22051736;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP936017.RAM56iN-YuxEpdv8yg8yz-QWfFCGTXmhMpqy7IqQDI13g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:49+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}