@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:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_head { this: np:hasAssertion dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_assertion; np:hasProvenance dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_provenance; np:hasPublicationInfo dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_publicationInfo; a np:Nanopublication . dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_assertion a np:Assertion . dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_provenance a np:Provenance . dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_publicationInfo a np:PublicationInfo . } dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_assertion { miriam-gene:1636 a ncit:C16612 . lld:C0009450 a ncit:C7057 . dgn-gda:DGN6d9a5a30eb14df47020dab09896c8786 sio:SIO_000628 miriam-gene:1636, lld:C0009450; a sio:SIO_001121 . } dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_provenance { dgn-np:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_assertion dcterms:description "[We used this method to analyze a) a highly polymorphic pentanucleotide repeat (CCTTT)(n) locus within the 5'-putative promoter region of the human inducible nitric oxide synthase gene (iNOS5) which is associated with diabetic complications and infectious diseases; b) a bi-allelic 27 bp VNTR region within intron 4 of endothelial nitric oxide gene (eNOS27) which is associated with hypertension in type 2 diabetes patients with coronary heart disease and excess risk of advanced diabetic nephropathy in type 1 diabetes patients and c) an insertion/deletion polymorphism within the gene encoding angiotensin-converting enzyme (ACE/ID) which is associated with cardiovascular pathology and nitric oxide activity, and is in strong linkage disequilibrium with functional variants.]. 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:12554058; 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:NP578404.RAMM7OARNK4eZS-_wjR_dh25MPMNLADw7G4XSmhVz1UAs130_publicationInfo { this: dcterms:created "2014-10-02T12:37:48+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }