@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM> .
@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:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_head {
  this: np:hasAssertion dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion ;
    np:hasProvenance dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_provenance ;
    np:hasPublicationInfo dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion a np:Assertion .
  dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_provenance a np:Provenance .
  dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0007102 a ncit:C7057 .
  dgn-gda:DGN191f7ecd740091fb6a8882af3e41ed8a sio:SIO_000628 miriam-gene:4524 , lld:C0007102 ;
    a sio:SIO_001121 .
}
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_provenance {
  dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion dcterms:description "[The hypothesis that these two pathways are the means by which folate modulates cancer risk is also supported by the epidemiological observation that a common polymorphism in the methylenetetrahydrofolate reductase (MTHFR; EC 1.5.1.20) gene differentially affects the relative risk of colon cancer depending on folate status, because MTHFR catalyzes the reaction that determines whether cellular folate is diverted into biological methylation or nucleotide synthesis.]. 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:12163703 ;
    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:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:20+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" .
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}