@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU> .
@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:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_head {
  this: np:hasAssertion dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_assertion ;
    np:hasProvenance dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_provenance ;
    np:hasPublicationInfo dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_assertion a np:Assertion .
  dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_provenance a np:Provenance .
  dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_assertion {
  miriam-gene:4314 a ncit:C16612 .
  lld:C0242698 a ncit:C7057 .
  dgn-gda:DGNea462959c08ecd65c973a80dd10efa86 sio:SIO_000628 miriam-gene:4314 , lld:C0242698 ;
    a sio:SIO_001122 .
}
dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_provenance {
  dgn-np:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_assertion dcterms:description "[ MMP-3 and MMP-9 polymorphisms contribute to variability in cardiac survival in HF patients. These data suggest that MMP genotyping could provide important additional information for refining risk stratification in patients with heart failure. MMP genotyping may help to select patients who could benefit from MMP inhibition.]. 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:15084374 ;
    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:NP54504.RALxd5DhCmXvFSeCA8iXSdk4Awl0EBDCy8ZCKflG6oqxU130_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> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}