@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU> .
@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:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_head {
  this: np:hasAssertion dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_assertion ;
    np:hasProvenance dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_provenance ;
    np:hasPublicationInfo dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_assertion a np:Assertion .
  dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_provenance a np:Provenance .
  dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_assertion {
  miriam-gene:4522 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGN60b01a701f770fe206484fb65f918728 sio:SIO_000628 miriam-gene:4522 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_provenance {
  dgn-np:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_assertion dcterms:description "[The objective of this study was to evaluate the role of folate intake (and intakes of related dietary components such as methionine), 35 SNPs in three FOCM pathway genes (MTHFD1, MTHFR, and TYMS), and their interactions on CRC risk in a population-based case-control study in Pennsylvania (686 cases, 740 controls).]. 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:23893618 ;
    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:NP537825.RA1GlwTgSKKt-JtkqsDd0VEnbS16CuecBhfXnnYCdyruU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:24+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" .
}