@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8> .
@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:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_head {
  this: np:hasAssertion dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_assertion ;
    np:hasProvenance dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_provenance ;
    np:hasPublicationInfo dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_assertion a np:Assertion .
  dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_provenance a np:Provenance .
  dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_assertion {
  miriam-gene:4709 a ncit:C16612 .
  lld:C0040038 a ncit:C7057 .
  dgn-gda:DGNaa0a7c116c795f6bc7a47cfeaf0d13cf sio:SIO_000628 miriam-gene:4709 , lld:C0040038 ;
    a sio:SIO_001121 .
}
dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_provenance {
  dgn-np:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_assertion dcterms:description "[Several polymorphisms of genes encoding for enzymes acting in the remethylation pathway of homocysteine metabolism, ie, methionine synthase (MS) A2756G, methylenetetrahydrofolate reductase (MTHFR) C677T and MTHFR A1298C, can cause increased homocysteine levels particularly in patients with deficiencies of folic acid, vitamin B6, or B12 and hence be potential risk factors for VTE.]. 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:11920232 ;
    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:NP550235.RA-SL1UuRNfciytDR8lTdu355SgqxkjRe2qinRuEQdHN8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}