@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ> .
@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:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_head {
  this: np:hasAssertion dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_assertion;
    np:hasProvenance dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_provenance;
    np:hasPublicationInfo dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_assertion a np:Assertion .
  
  dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_provenance a np:Provenance .
  
  dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0155626 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_provenance {
  dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_assertion dcterms:description
      "[We have examined the prevalence of the C677T and A1298C single nucleotide polymorphisms (SNPs) in the methylenetetrahydrofolate reductase (MTHFR) gene in healthy Tamilians and in patients with acute myocardial infarction and related this polymorphism to plasma homocysteine concentrations, serum folate, serum cobalamin and riboflavin status.]. 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:17412321;
    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:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}