@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A> .
@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:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_head {
  this: np:hasAssertion dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_assertion;
    np:hasProvenance dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_provenance;
    np:hasPublicationInfo dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_assertion a np:Assertion .
  
  dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_provenance a np:Provenance .
  
  dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0011570 a ncit:C7057 .
  
  dgn-gda:DGN2284dee64a846299d70456629c77f1f2 sio:SIO_000628 miriam-gene:4524, lld:C0011570;
    a sio:SIO_001121 .
}

dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_provenance {
  dgn-np:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_assertion dcterms:description
      "[A common C677T polymorphism in MTHFR has been associated with an increased risk for the development of cardiovascular disease, Alzheimer's disease, and depression in adults, and of neural tube defects in the fetus.]. 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:23116396;
    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:NP192326.RAQehSkecugeuxG4CKiQ5PQq0SM1VLvEalKLoOO700a2A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}