@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg> .
@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:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_head {
   this: np:hasAssertion dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_assertion ;
    np:hasProvenance dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_provenance ;
    np:hasPublicationInfo dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_assertion a np:Assertion .
  dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_provenance a np:Provenance .
  dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_assertion {
   miriam-gene:4709 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN65aebf469fa10aa60da68e122cbdcec5 sio:SIO_000628 miriam-gene:4709 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_provenance {
   dgn-np:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_assertion dcterms:description "[Using a cohort we have been studying in Linxian since 1985, we examined the relationship between incident ESCC and GCA cancers and three polymorphisms in two genes that code for enzymes that require folate and B(12) as cofactors: methionine synthase reductase (MTRR) A66G and methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C.]. 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:14652285 ;
    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:NP828338.RAyR16lYa0aEJmwPwmtR5gS7y99v4Ne7e0USqWREWR0Fg130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:27+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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}