@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:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_head { this: np:hasAssertion dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_assertion; np:hasProvenance dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_provenance; np:hasPublicationInfo dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_publicationInfo; a np:Nanopublication . dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_assertion a np:Assertion . dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_provenance a np:Provenance . dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_publicationInfo a np:PublicationInfo . } dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_assertion { miriam-gene:3119 a ncit:C16612 . lld:C0035078 a ncit:C7057 . dgn-gda:DGN57ea916b116586b1d25705a8ef723334 sio:SIO_000628 miriam-gene:3119, lld:C0035078; a sio:SIO_001121 . } dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_provenance { dgn-np:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_assertion dcterms:description "[The frequency of HLA-DQB1*0602 was decreased in IgA-N patients (3.6% vs 10.2%, Pc = 0.04, RR = 0.36), suggesting a protective effect of this allele for IgA-N. Kaplan-Meyer analysis with the Cox-proportional hazard model revealed a shorter time between diagnosis and renal failure in patients with the B allele for the al gene hs1,2 enhancer (p = 0.04).]. 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:12005241; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP453746.RAlmJ09rsP7ZT1tz1I20gfXSThHniGa-6rJDw5P-FGNBk130_publicationInfo { this: dcterms:created "2015-08-25T14:42:06+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }