@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0> .
@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:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_head {
  this: np:hasAssertion dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_assertion;
    np:hasProvenance dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_provenance;
    np:hasPublicationInfo dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_assertion a np:Assertion .
  
  dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_provenance a np:Provenance .
  
  dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGNafeda7d7290d19b86b915819238c0816 sio:SIO_000628 miriam-gene:4524, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_provenance {
  dgn-np:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_assertion dcterms:description
      "[The prevalence of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in Asian Indians from India was determined and the association of the mutant allele with coronary artery disease (CAD) was evaluated in a case-control study.]. 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:11940092;
    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:NP212685.RAq0PdFfwWq6Tq0ME-eWadtw-E2dSD2Y1UwjlluSp30K0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}