@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY> .
@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:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_head {
  this: np:hasAssertion dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion ;
    np:hasProvenance dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_provenance ;
    np:hasPublicationInfo dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion a np:Assertion .
  dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_provenance a np:Provenance .
  dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C1333762 a ncit:C7057 .
  dgn-gda:DGN25b9d91a17f79f5096a745411114db61 sio:SIO_000628 miriam-gene:4524 , lld:C1333762 ;
    a sio:SIO_001121 .
}
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_provenance {
  dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion dcterms:description "[In most studies, the MTHFR 677TT (variant) genotype, which is associated with reduced enzyme activity, was associated with an increased risk of esophageal squamous cell carcinoma, gastric cardia adenocarcinoma, noncardia gastric cancer, gastric cancer (all subsites), and pancreatic cancer; all but one of 22 odds ratios were >1, of which 13 estimates were statistically significant.]. 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:17030196 ;
    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:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:36+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" .
}