@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g> .
@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:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_head {
  this: np:hasAssertion dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_assertion;
    np:hasProvenance dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_provenance;
    np:hasPublicationInfo dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_assertion a np:Assertion .
  
  dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_provenance a np:Provenance .
  
  dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_assertion {
  miriam-gene:4548 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_provenance {
  dgn-np:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_assertion dcterms:description
      "[Our results suggest that neither single mutation nor combined mutations in MTHFR C677T, CBS 844ins68 and MS A2756G represent an independent risk factor for increasing IS and coronary artery disease risks in Chinese population.]. 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:11672761;
    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:NP520462.RAprwg1CabUvs6u506hkwKhVNE95KBnh4F0UeGitRbc7g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:10+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" .
}