@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI> .
@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 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:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_head {
  this: np:hasAssertion dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_assertion;
    np:hasProvenance dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_provenance;
    np:hasPublicationInfo dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_assertion a np:Assertion .
  
  dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_provenance a np:Provenance .
  
  dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_assertion {
  miriam-gene:5981 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGNfd327685aeaa8c0590073729f72f427e sio:SIO_000628 miriam-gene:5981, lld:C0013080;
    a sio:SIO_001122 .
}

dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_provenance {
  dgn-np:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_assertion dct:description
      "[The aim of the present study was to investigate the effect of polymorphisms C677T and A1298C in the methylenetetrahydrofolate reductase (MTHFR) gene, A2756G in methionine synthase reductase (MTR) gene and A80G in reduced folate carrier 1 (RFC1) gene, and plasma homocysteine (Hcy), on the maternal risk for Down syndrome (DS).]. 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:18273817;
    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:NP82302.RAwrzJjhNoAhmpeVCiJP5WAQP1j7Eto0osj9XnJPt2LfI130_publicationInfo {
  this: dct:created "2014-10-02T12:32:40+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}