@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs> .
@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:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_head {
  this: np:hasAssertion dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion;
    np:hasProvenance dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance;
    np:hasPublicationInfo dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion a np:Assertion .
  
  dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance a np:Provenance .
  
  dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion {
  miriam-gene:6470 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNbaa8211b6a512a4bda2638bed9f3ae20 sio:SIO_000628 miriam-gene:6470, lld:C0014544;
    a sio:SIO_001122 .
}

dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance {
  dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_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:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:46+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" .
}