@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw> .
@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:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_head {
  this: np:hasAssertion dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_assertion ;
    np:hasProvenance dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_provenance ;
    np:hasPublicationInfo dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_provenance a np:Provenance .
  dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_assertion {
  miriam-gene:183 a ncit:C16612 .
  lld:C0155626 a ncit:C7057 .
  dgn-gda:DGN48ec3262063d8113b94e2c74f533f494 sio:SIO_000628 miriam-gene:183 , lld:C0155626 ;
    a sio:SIO_001121 .
}
dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_provenance {
  dgn-np:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_assertion dcterms:description "[The objective of the study was to explore the role of a genetic variant of angiotensinogen (AGT), M235T, as an independent risk factor for acute myocardial infarction (AMI) and to investigate the possible association with the severity of coronary artery disease (CAD), estimated on the basis of the number of coronary stenoses and critical arterial occlusions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP165371.RAwnuJURApaq7l26ABkhYN4HN-BomNOuJ1BsuywJdNqKw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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