@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg> .
@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:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_head {
  this: np:hasAssertion dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion ;
    np:hasProvenance dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_provenance ;
    np:hasPublicationInfo dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion a np:Assertion .
  dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_provenance a np:Provenance .
  dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion {
  miriam-gene:5981 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGN3bf9e78f1f3cf16a9a621e957084268c sio:SIO_000628 miriam-gene:5981 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_provenance {
  dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion dcterms:description "[Conversely, for women over 50, the risk of breast cancer development was statistically associated with the MTHFR 677CT genotype, but especially significant was risk associated with the presence of the polymorphic allele of cSHMT C1420T (P = 0.0120) and the protective effect associated with the RFC1 G80A polymorphism allele (P = 0.0021), was restrict to this age group.]. 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:22134752 ;
    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:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:16+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" .
}