@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:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_head { this: np:hasAssertion dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_assertion; np:hasProvenance dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_provenance; np:hasPublicationInfo dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_publicationInfo; a np:Nanopublication . dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_assertion a np:Assertion . dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_provenance a np:Provenance . dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_publicationInfo a np:PublicationInfo . } dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_assertion { miriam-gene:4700 a ncit:C16612 . lld:C2931161 a ncit:C7057 . dgn-gda:DGNba8cfb7885ad3c17078153ca98a2c52f sio:SIO_000628 miriam-gene:4700, lld:C2931161; a sio:SIO_001121 . } dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_provenance { dgn-np:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_assertion dcterms:description "[There are strong indications for involvement of genetic factors in development of the disease and the frequency of several extended major histocompatibility complex haplotypes (including HLA-A1, B8, DR3, DQ2) have previously been shown to be increased among Caucasian patients with IgAD.PCR was used to type HLA B, DR, and DQ alleles in 29 Iranian individuals with IgAD and 299 Swedish individuals with IgAD.The results indicate a strong association with the HLA B14, DR1 alleles in Iranian subjects and HLA B8, B12, B13, B14, B40, DR1, DR3, DR7, DQ2 and DQ5 alleles in Swedish subjects.Differences in HLA association of IgAD in Iran and Sweden confirm the notion of a genetic background of the disease and that multiple, potentially different genes within the MHC region might be involved in the pathogenesis of IgAD in different ethnic groups.]. 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:19052350; 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:NP203835.RAWoJo9qwgc7d7xJbQCHf5PZnpIfv5wi3lLbGal4-T2DU130_publicationInfo { this: dcterms:created "2014-10-02T12:33:52+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" . }