@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_head { this: np:hasAssertion dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_assertion; np:hasProvenance dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_provenance; np:hasPublicationInfo dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_publicationInfo; a np:Nanopublication . dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_assertion a np:Assertion . dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_provenance a np:Provenance . dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_publicationInfo a np:PublicationInfo . } dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_assertion { miriam-gene:4321 a ncit:C16612 . lld:C0005684 a ncit:C7057 . dgn-gda:DGN1fc44a14fce5c914f8e26a633617ffa3 sio:SIO_000628 miriam-gene:4321, lld:C0005684; a sio:SIO_001122 . } dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_provenance { dgn-np:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_assertion dcterms:description "[The MMP-9 microsatellite > or =24 CA repeat allele and the MMP-12-82 GG polymorphisms were associated with invasive bladder cancer risk odds ratio (OR), 2.60; 95% confidence interval (95% CI), 1.07-6.26; and OR, 4.59; 95% CI, 1.21-17.32, respectively.]. 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:17178858; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP104524.RAj8Hje0HhjL0hvWqF1f1DVGaqQsTGH19zMkCHjtuT8f4130_publicationInfo { this: dcterms:created "2016-05-13T12:42:35+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }