@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:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_head { this: np:hasAssertion dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_assertion; np:hasProvenance dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_provenance; np:hasPublicationInfo dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_publicationInfo; a np:Nanopublication . dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_assertion a np:Assertion . dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_provenance a np:Provenance . dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_publicationInfo a np:PublicationInfo . } dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_assertion { miriam-gene:3553 a ncit:C16612 . lld:C0017154 a ncit:C7057 . dgn-gda:DGN2907d6cc72fb6ed3e6ca5def11581ea8 sio:SIO_000628 miriam-gene:3553, lld:C0017154; a sio:SIO_001121 . } dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_provenance { dgn-np:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_assertion dcterms:description "[When subjects were divided into the 3 groups according to the histological severity of gastric mucosal atrophy: the non-atrophic gastritis (NA) group (atrophy score=0 and metaplasia score=0), the severe atrophic gastritis (SA) group (atrophy score>=2 or metaplasia score>=2), and the mild atrophic gastritis (MA) group (all others), synergistic effect was found between numbers of IL-1β-31C, IL-1β-511T variant alleles with co-factors on the development of gastric atrophy in the antrum (gender + H. pylori + number of IL-1β-31C allele: p=0.001, age + gender + H. pylori + number of IL-1β-31C allele: p=0.0008, gender + H. pylori + number of IL-1β-511T allele: p=0.016, age + gender + H. pylori + number of IL-1β-511T allele: p=0.013), while such association was found for TNF-α-857 T allele in the antrum and all genotypes in the corpus.]. 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:23169178; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1029983.RAqVWtE3XzuB1VrV4APzUr4Iyf8YkpUb_zYRVLQrV2zjA130_publicationInfo { this: dcterms:created "2016-05-13T12:49:32+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" . }