@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4> .
@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:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_head {
  this: np:hasAssertion dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_assertion ;
    np:hasProvenance dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_provenance ;
    np:hasPublicationInfo dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_assertion a np:Assertion .
  dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_provenance a np:Provenance .
  dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_assertion {
  miriam-gene:4321 a ncit:C16612 .
  lld:C0699885 a ncit:C7057 .
  dgn-gda:DGNa165e45c45ef372357f3d95d95918613 sio:SIO_000628 miriam-gene:4321 , lld:C0699885 ;
    a sio:SIO_001121 .
}
dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_provenance {
  dgn-np:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_assertion dcterms:description "[Using a case-only study, we examined the association of 11 single-nucleotide polymorphisms and one microsatellite polymorphism in MMP genes MMP1, MMP2, MMP3, MMP8, MMP9, and MMP12 with the risk of invasive bladder cancer in 243 Caucasian patients with muscle invasive compared with 315 Caucasian patients with superficial disease.]. 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:17473191 ;
    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:NP696220.RAx9BkgYIVqW2Vn8ELb_cd1u1tlQcy4GlSdWHbVrvLYY4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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" .
}