@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk> .
@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:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_head {
  this: np:hasAssertion dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_assertion ;
    np:hasProvenance dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_provenance ;
    np:hasPublicationInfo dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_assertion a np:Assertion .
  dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_provenance a np:Provenance .
  dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGN18758ff3f71a1a8bb19a506cbe907059 sio:SIO_000628 miriam-gene:4524 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_provenance {
  dgn-np:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_assertion dcterms:description "[These results, which need to be confirmed in other studies, suggest that the MTHFR val/val polymorphism, which has been previously inversely associated with risk of colorectal cancer, plays a role only in a late stage (adenoma-->carcinoma) of colorectal tumorigenesis, and/or may protect against malignant transformation in the subset of benign adenomas, which may progress to malignancy.]. 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:9886567 ;
    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:NP251791.RAQFkRvcMlJ6ah5PAM4GnA7mTSylbzn0-he12h3TR5PXk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:20+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" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}