@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_head {
  this: np:hasAssertion dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_assertion ;
    np:hasProvenance dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_provenance ;
    np:hasPublicationInfo dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_assertion a np:Assertion .
  dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_provenance a np:Provenance .
  dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0013080 a ncit:C7057 .
  dgn-gda:DGN04aa87e78097ce52e9729d671efb4c79 sio:SIO_000628 miriam-gene:4524 , lld:C0013080 ;
    a sio:SIO_001122 .
}
dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_provenance {
  dgn-np:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_assertion dcterms:description "[With the purpose of evaluating this relationship, we compared the frequencies of 677C&gt;T and 1298A&gt;C polymorphisms in the methylenetetrahydrofolate reductase gene (MTHFR) and 66A&gt;G in the methionine synthase reductase gene (MTRR) between 103 young mothers of Down syndrome (DS) individuals and 108 control mothers, whose offspring was karyotypically normal, correlating it with an estimative of folate and - related micronutrients levels intake.]. 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:19096127 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP710256.RATFOrqVK9L-Pk0Rpg62q_vwW_1fU1iovJLJ8wFtThW4A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:07+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:disgenetv3.0rdf ;
    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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}