@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ> .
@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:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_head {
  this: np:hasAssertion dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_assertion ;
    np:hasProvenance dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_assertion a np:Assertion .
  dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_provenance a np:Provenance .
  dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_assertion {
  miriam-gene:4314 a ncit:C16612 .
  lld:C0005684 a ncit:C7057 .
  dgn-gda:DGN128caf97cb75b003d24d57aa7a59ffb8 sio:SIO_000628 miriam-gene:4314 , lld:C0005684 ;
    a sio:SIO_001121 .
}
dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_provenance {
  dgn-np:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_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:NP621129.RAOg3V9nVylhxeQtR8GMMJWWPXoLMvh7wWirrHhF76kmQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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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    pav:version "v2.1.0.0" .
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}