@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg> .
@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:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_head {
  this: np:hasAssertion dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_assertion;
    np:hasProvenance dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_provenance;
    np:hasPublicationInfo dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_assertion a np:Assertion .
  
  dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_provenance a np:Provenance .
  
  dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_assertion {
  miriam-gene:7298 a ncit:C16612 .
  
  lld:C0007113 a ncit:C7057 .
  
  dgn-gda:DGN6d91f398f23bf54f36d3ed39454ac0e0 sio:SIO_000628 miriam-gene:7298, lld:C0007113;
    a sio:SIO_001121 .
}

dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_provenance {
  dgn-np:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_assertion dcterms:description
      "[The objective of the present study was to evaluate whether germline methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms as well as polymorphisms in the thymidylate synthase gene promoter, namely the variable number tandem repeat polymorphism (TS VNTR) and the intrarepeat G to C single nucleotide polymorphism (TS SNP), are predictive markers of tumor regression in rectal cancer patients following preoperative chemoradiotherapy.]. 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:17047490;
    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:NP378452.RAmliTmc8TCkXsOYrFr-ki-eUHvDq-QZor4Btsa1ePhSg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:41+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" .
}