@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ> .
@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:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_head {
  this: np:hasAssertion dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion ;
    np:hasProvenance dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion a np:Assertion .
  dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_provenance a np:Provenance .
  dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0034065 a ncit:C7057 .
  dgn-gda:DGN487c90b2853c1f1995f8aedeb55c0c1e sio:SIO_000628 miriam-gene:4524 , lld:C0034065 ;
    a sio:SIO_001121 .
}
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_provenance {
  dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion dcterms:description "[We measured concentrations of homocysteine, methionine, and folate in plasma, total folate and methylfolate in red-blood cells, and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T genotype and other known risk factors for venous thromboembolic disease in 243 patients with deep vein thrombosis or pulmonary embolism and controls matched for sex and age.]. 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:11888585 ;
    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:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}