@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:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_head { this: np:hasAssertion dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_assertion; np:hasProvenance dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_provenance; np:hasPublicationInfo dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_publicationInfo; a np:Nanopublication . dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_assertion a np:Assertion . dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_provenance a np:Provenance . dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_publicationInfo a np:PublicationInfo . } dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_assertion { miriam-gene:114548 a ncit:C16612 . lld:C0013595 a ncit:C7057 . dgn-gda:DGN297a1a23ce1129c6c6ed534e32b1adf7 sio:SIO_000628 miriam-gene:114548, lld:C0013595; a sio:SIO_001121 . } dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_provenance { dgn-np:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_assertion dcterms:description "[We evaluated the possible association of five single nucleotide polymorphisms (SNPs), two in NLRP1 gene and three in NLRP3 gene, in pediatric patients from the north eastern region of Brazil affected by type-1 diabetes (T1D, n = 196), celiac disease (CD, n = 59), and atopic dermatitis (AD, n = 165), and in healthy individuals (n = 192).]. 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:20370570; 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:NP964565.RA5bQL0mkdphGe0SmySkU9L7YtN_DQQzlLuf2HPoswlsA130_publicationInfo { this: dcterms:created "2015-08-25T14:47:29+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" . }