@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:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_head { this: np:hasAssertion dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_assertion; np:hasProvenance dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_provenance; np:hasPublicationInfo dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_publicationInfo; a np:Nanopublication . dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_assertion a np:Assertion . dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_provenance a np:Provenance . dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_publicationInfo a np:PublicationInfo . } dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_assertion { miriam-gene:5175 a ncit:C16612 . lld:C1561643 a ncit:C7057 . dgn-gda:DGNbf5bed46c949fec478e7dd1fd9ad50e0 sio:SIO_000628 miriam-gene:5175, lld:C1561643; a sio:SIO_001121 . } dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_provenance { dgn-np:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_assertion dcterms:description "[The Chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that ten different polymorphisms were associated (P<0.05) with the prevalence of CKD in high- or low-risk subjects: the -519Aright curved arrow G polymorphism of MMP1, the 1061Aright curved arrow G (Ile405Val) polymorphism of CETP, the Aright curved arrow G (Lys45Glu) polymorphism of MMP3, the -219Gright curved arrow T polymorphism of APOE, the Aright curved arrow G (Ile1205Val) polymorphism of COL3A1, the -863Cright curved arrow A polymorphism of TNF, and the 1454Cright curved arrow G (Leu125Val) polymorphism of PECAM1 in high-risk subjects; and the 1167Cright curved arrow T (Asn389Asn) polymorphism of TGFBR2, the 2386Aright curved arrow G (Ile796Val) polymorphism of SCAP, and the TAAAright curved arrow del polymorphism of PDE4D in low-risk subjects.]. 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:19424605; 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:NP832060.RAVDEB-SGrG-r4jKENngp7J404P_HDYmCNoKXGy9wcHxU130_publicationInfo { this: dcterms:created "2014-10-02T12:40:29+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" . }