@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto> .
@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:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_head {
   this: np:hasAssertion dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_assertion ;
    np:hasProvenance dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_provenance ;
    np:hasPublicationInfo dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_assertion a np:Assertion .
  dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_provenance a np:Provenance .
  dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_assertion {
   miriam-gene:23531 a ncit:C16612 .
  lld:C0013080 a ncit:C7057 .
  dgn-gda:DGNfa9f315e0dd97045310e0b16c50a3ba2 sio:SIO_000628 miriam-gene:23531 , lld:C0013080 ;
    a sio:SIO_001121 .
}
dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_provenance {
   dgn-np:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_assertion dcterms:description "[This study evaluated the influence of a 19-base pair (bp) deletion polymorphism in intron-1 of the dihydrofolate reductase (DHFR) gene on the maternal risk of DS, and investigated the association between this polymorphism and variations in the concentrations of serum folate and plasma homocysteine (Hcy) and plasma methylmalonic acid (MMA).]. 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:21120433 ;
    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:NP260350.RAUpMTpsAR_8ZhvSSf8VAu5oSm0O3ULsnnOdPKbskdtto130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:25+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" .
}