@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc> .
@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:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_head {
   this: np:hasAssertion dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_assertion ;
    np:hasProvenance dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_provenance ;
    np:hasPublicationInfo dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_assertion a np:Assertion .
  dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_provenance a np:Provenance .
  dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_assertion {
   miriam-gene:4092 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGN2037a95c2a6bb258efd169bc33ac645b sio:SIO_000628 miriam-gene:4092 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_provenance {
   dgn-np:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_assertion dcterms:description "[We consider 16 independent variants at 13 loci (MUTYH, MTHFR, SMAD7, and common variants tagging the loci 8q24, 8q23.3, 11q23.1, 14q22.2, 1q41, 20p12.3, 20q13.33, 3q26.2, 16q22.1, and 19q13.1) to have the most highly credible associations with colorectal cancer, with all variants except those in MUTYH and 19q13.1 reaching genome-wide statistical significance in at least one meta-analysis model.]. 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:23019048 ;
    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:NP366121.RA-fxzY6fL6dmI957jw-NDb7b1J-5pok5hjb31St4L5Pc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:34+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> ;
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}