@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_head {
  this: np:hasAssertion dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_assertion ;
    np:hasProvenance dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_provenance ;
    np:hasPublicationInfo dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_assertion a np:Assertion .
  dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_provenance a np:Provenance .
  dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_assertion {
  miriam-gene:59286 a ncit:C16612 .
  lld:C0010068 a ncit:C7057 .
  dgn-gda:DGNb5e0d105f276a1d8a37346bf4c6a46ee sio:SIO_000628 miriam-gene:59286 , lld:C0010068 ;
    a sio:SIO_001122 .
}
dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_provenance {
  dgn-np:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_assertion dcterms:description "[The merits of two techniques, molecular beacon and amplification effect of enzymatic color, are successfully combined, and the technique is simple, sensitive and specific, to detect and compare the methylenetetrahydrofolate reductase (MTHFR) Gene C677T mutation of subjects between coronary heart disease (CHD) and control group.]. 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:21802936 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP934965.RAVH7QMNdD10YYZ9K7QYY2iJjuLaKgF44F1sPMIC7J1Rk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:11+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
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}