@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A> .
@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:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_head {
  this: np:hasAssertion dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_assertion;
    np:hasProvenance dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_provenance;
    np:hasPublicationInfo dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_assertion a np:Assertion .
  
  dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_provenance a np:Provenance .
  
  dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN2177e017df49049a92000e3689d60617 sio:SIO_000628 miriam-gene:4524, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_provenance {
  dgn-np:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_assertion dcterms:description
      "[We tested whether the polymorphisms of the methylenetetrahydrofolate reductase gene, MTHFR C677T and A1298C, the methionine synthase gene, MTR A2756G, the methionine synthase reductase gene, MTRR A66G, and the thymidylate synthase gene, TYMS 2R-->3R, involved in folate and methionine metabolism, altered the risk for multiple myeloma (MM).]. 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:17655928;
    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:NP226004.RAbCA1m7nTwqnc70KKhs0c1ebn1jacIl4ARGvq5czju0A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:05+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" .
}