@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk> .
@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:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_head {
  this: np:hasAssertion dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion;
    np:hasProvenance dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance;
    np:hasPublicationInfo dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion a np:Assertion .
  
  dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance a np:Provenance .
  
  dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion {
  miriam-gene:4552 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNf76d9c6b7ba0aaac57d8adeaa514a949 sio:SIO_000628 miriam-gene:4552, lld:C0014544;
    a sio:SIO_001122 .
}

dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance {
  dgn-np:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion dcterms:description
      "[To investigate this further, a new cohort of women with epilepsy has been identified from maternity hospital records and genotyped for polymorphisms in MTHFR, serine hydroxymethyl transferase (SHMT1), methionine synthase (MTR) and methionine synthase reductase (MTRR).]. 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:17904392;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+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" .
}