@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync> .
@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:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_head {
  this: np:hasAssertion dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion ;
    np:hasProvenance dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_provenance ;
    np:hasPublicationInfo dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion a np:Assertion .
  dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_provenance a np:Provenance .
  dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGNbae60f37fcbc3be98d6b7169fd611fb6 sio:SIO_000628 miriam-gene:4524 , lld:C0006142 ;
    a sio:SIO_001122 .
}
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_provenance {
  dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion dcterms:description "[Encouraged by recent studies on the MTHFR 677C>T polymorphism and breast cancer risk that suggested an association of the 677 TT genotype with increased breast cancer susceptibility in premenopausal women, we performed an analysis of the relationship between breast cancer risk and the MTHFR 677C>T polymorphism in 210 premenopausal breast cancer patients and sex- and agematched healthy control subjects.]. 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:17453338 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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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}