@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:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_head { this: np:hasAssertion dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_assertion; np:hasProvenance dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_provenance; np:hasPublicationInfo dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_publicationInfo; a np:Nanopublication . dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_assertion a np:Assertion . dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_provenance a np:Provenance . dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_publicationInfo a np:PublicationInfo . } dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_assertion { miriam-gene:3596 a ncit:C16612 . lld:C0004096 a ncit:C7057 . dgn-gda:DGNd9abf832ad6a36695b014f5552a26000 sio:SIO_000628 miriam-gene:3596, lld:C0004096; a sio:SIO_001122 . } dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_provenance { dgn-np:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_assertion dcterms:description "[A novel variant of human IL-13, Gln110Arg, on chromosome 5q31, associated with asthma rather than IgE levels in case-control populations from Britain and Japan [peak odds ratio (OR) = 2.31, 95% CI 1.33-4.00]; the variant also predicted asthma and higher serum IL-13 levels in a general, Japanese paediatric population.]. 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:10699178; 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:NP276847.RA5gwXqrgV1i3_T9PlIrEhCFbcANIZfUUChOw6KSzS49s130_publicationInfo { this: dcterms:created "2016-05-13T12:43:51+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" . }