@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s> .
@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:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_head {
  this: np:hasAssertion dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion;
    np:hasProvenance dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_provenance;
    np:hasPublicationInfo dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion a np:Assertion .
  
  dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_provenance a np:Provenance .
  
  dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion {
  miriam-gene:5981 a ncit:C16612 .
  
  lld:C3495426 a ncit:C7057 .
  
  dgn-gda:DGN8a1fd1850f957e975f490fd61a207467 sio:SIO_000628 miriam-gene:5981, lld:C3495426;
    a sio:SIO_001121 .
}

dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_provenance {
  dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion dcterms:description
      "[The purposes of this study were to explore whether hyperhomocysteinemia was related to MTX administration and toxicity and whether homocysteine or MTX toxicity differed by methylenetetrahydrofolate reductase (MTHFR) or reduced folate carrier (RFC) genetic polymorphisms.]. 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:12915598;
    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:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:43+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" .
}