@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ> .
@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:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_head {
  this: np:hasAssertion dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_assertion;
    np:hasProvenance dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_provenance;
    np:hasPublicationInfo dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_assertion a np:Assertion .
  
  dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_provenance a np:Provenance .
  
  dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0240912 a ncit:C7057 .
  
  dgn-gda:DGNb78788a13d8b71ca51dcacc17d6326ae sio:SIO_000628 miriam-gene:4524, lld:C0240912;
    a sio:SIO_001121 .
}

dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_provenance {
  dgn-np:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_assertion dcterms:description
      "[We report three patients with cerebral vein thrombosis (CVT) in which the only risk factor we were able to identify was increased blood homocysteine levels and the C677T polymorphism in both alleles of the methylene tetrahydrofolate reductase MTHFR gene.]. 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:12522678;
    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:NP329643.RABYqadt_MNc61ZNwJbCJpSwuznAudnqq8aoYmH3ouJFQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:14+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" .
}