@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ> .
@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:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_head {
  this: np:hasAssertion dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_assertion;
    np:hasProvenance dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_provenance;
    np:hasPublicationInfo dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_assertion a np:Assertion .
  
  dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_provenance a np:Provenance .
  
  dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_assertion {
  miriam-gene:7126 a ncit:C16612 .
  
  lld:C0028754 a ncit:C7057 .
  
  dgn-gda:DGNd80bd35dbde8f9f318b0997fb4423dfc sio:SIO_000628 miriam-gene:7126, lld:C0028754;
    a sio:SIO_001121 .
}

dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_provenance {
  dgn-np:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_assertion dcterms:description
      "[To investigate the frequencies of C677T polymorphism in MTHFR gene and G80A polymorphism in RFC gene in obese and no obese Tunisian children and to assess their relation with homocysteine (tHcy), folate and vitamin B12 levels.]. 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:21681722;
    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:NP837096.RAshEdeD1Q98gMS3zrvQJPFRdhgMue4-R8e10_NMCVuyQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:32+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}