@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M> .
@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:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_head {
  this: np:hasAssertion dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion;
    np:hasProvenance dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_provenance;
    np:hasPublicationInfo dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion a np:Assertion .
  
  dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_provenance a np:Provenance .
  
  dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0747845 a ncit:C7057 .
  
  dgn-gda:DGNbcb900b505bcfb20e61cd93abe6f37e3 sio:SIO_000628 miriam-gene:4524, lld:C0747845;
    a sio:SIO_001122 .
}

dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_provenance {
  dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion dcterms:description
      "[The methylenetetrahydrofolate reductase (MTHFR) gene C677T and A1298C polymorphisms are commonly associated with defects in folate dependent homocysteine metabolism and have been implicated as risk factors for recurrent embryo loss in early pregnancy.]. 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:11938441;
    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:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:24+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}