@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw> .
@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:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_head {
   this: np:hasAssertion dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_assertion ;
    np:hasProvenance dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_provenance ;
    np:hasPublicationInfo dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_assertion a np:Assertion .
  dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_provenance a np:Provenance .
  dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_assertion {
   miriam-gene:4312 a ncit:C16612 .
  lld:C1276061 a ncit:C7057 .
  dgn-gda:DGN0fa815ab77dbadc9ebc140c88acb05e1 sio:SIO_000628 miriam-gene:4312 , lld:C1276061 ;
    a sio:SIO_001121 .
}
dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_provenance {
   dgn-np:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_assertion dcterms:description "[MMP-1 (-1607 G in/del), MMP-3 (-1171 A in/del), and MMP-9 microsatellite ((13-26) CA repeats around -90) PMs have been determined (i) in 204 patients with cerebrovascular disease to assess the association with features of vulnerability in carotid plaques and prevalence of stroke, (ii) in 208 patients with UA/NSTEMI to assess the association with in-hospital clinical outcome.]. 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:21232745 ;
    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:NP926738.RAVgcz0uZrP1RAdvBs2flfqLSXGK9V11weYWF1aOftIHw130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:28+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" .
}