@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ> .
@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:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_head {
  this: np:hasAssertion dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion ;
    np:hasProvenance dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion a np:Assertion .
  dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_provenance a np:Provenance .
  dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion {
  miriam-gene:4314 a ncit:C16612 .
  lld:C0010054 a ncit:C7057 .
  dgn-gda:DGN03b34e71cedb2af83800fce4c5e0047e sio:SIO_000628 miriam-gene:4314 , lld:C0010054 ;
    a sio:SIO_001122 .
}
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_provenance {
  dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion dcterms:description "[ There is a low frequency of the stromelysin-1 promoter 5A allele in the Chinese population in Taiwan. How stromelysin-1 5A/6A polymorphism affects ISR appears to be linked to angina status. These results merit further study to identify patients carrying genotypes which put them at increased risk of ISR, and which matrix metalloproteinase inhibitors or drug-eluting stents are more effective for those at risk.]. 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:16323393 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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> ;
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}