@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg> .
@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:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_head {
   this: np:hasAssertion dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_assertion ;
    np:hasProvenance dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_provenance ;
    np:hasPublicationInfo dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_assertion a np:Assertion .
  dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_provenance a np:Provenance .
  dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_assertion {
   miriam-gene:4524 a ncit:C16612 .
  lld:C0235974 a ncit:C7057 .
  dgn-gda:DGNb273ad0efc211ff143f9c63f7ae4d935 sio:SIO_000628 miriam-gene:4524 , lld:C0235974 ;
    a sio:SIO_001121 .
}
dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_provenance {
   dgn-np:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_assertion dcterms:description "[We found that functional polymorphisms in methylenetetrahydrofolate reductase (MTHFR) and thymidylate synthase (TS), two key enzymes involved in folate and methyl group metabolism, were significantly associated with increased risk of esophageal squamous cell carcinoma, gastric cardia carcinoma, and pancreatic carcinoma.]. 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:17684410 ;
    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:NP793119.RAiB2lJyHN89t7N3BcNEkim7vvZoOdQXllwW6QHD4AHJg130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:07+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" .
}