@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM> .
@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:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_head {
  this: np:hasAssertion dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_assertion;
    np:hasProvenance dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_provenance;
    np:hasPublicationInfo dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_assertion a np:Assertion .
  
  dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_provenance a np:Provenance .
  
  dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0016412 a ncit:C7057 .
  
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dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_provenance {
  dgn-np:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_assertion dcterms:description
      "[Hyperhomocysteinemia, a risk factor for vascular disease, is related to vitamin B12, vitamin B6, and especially folate deficiency, or to genetic factors such as mutations in methylenetetrahydrofolate reductase (MTHFR), an enzyme involved in the remethylation pathway of homocysteine to methionine.]. 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:9826223;
    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:NP1409444.RAGjn_ClGaWUCO1vs1REXEfeb0zwjGsW1gGdiOP8M_bKM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:25+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
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    pav:version "v4.0.0.0" .
  
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}