@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw> .
@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:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_head {
  this: np:hasAssertion dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_assertion ;
    np:hasProvenance dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_provenance ;
    np:hasPublicationInfo dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_assertion {
  miriam-gene:59286 a ncit:C16612 .
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dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_provenance {
  dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_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 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP762857.RAMciafGsjQPQtJ_DbEuOzHX8ycep3uRcOUpHt0uOlbIw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:42+02:00"^^xsd:dateTime ;
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    dcterms:rightsHolder dgn-void:IBIGroup ;
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