@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:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_head { this: np:hasAssertion dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_assertion; np:hasProvenance dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_provenance; np:hasPublicationInfo dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_publicationInfo; a np:Nanopublication . dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_assertion a np:Assertion . dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_provenance a np:Provenance . dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_publicationInfo a np:PublicationInfo . } dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_assertion { miriam-gene:56946 a ncit:C16612 . lld:C0004096 a ncit:C7057 . dgn-gda:DGN2a57964a0ec7e443facba5243b743b39 sio:SIO_000628 miriam-gene:56946, lld:C0004096; a sio:SIO_001122 . } dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_provenance { dgn-np:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_assertion dcterms:description "[The IL6R association further supports the hypothesis that cytokine signalling dysregulation affects asthma risk, and raises the possibility that an IL6R antagonist (tocilizumab) may be effective to treat the disease, perhaps in a genotype-dependent manner. Results for the 11q13.5 locus suggest that it directly increases the risk of allergic sensitisation which, in turn, increases the risk of subsequent development of asthma. Larger or more functionally focused studies are needed to characterise the many loci with modest effects that remain to be identified for asthma.]. 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:21907864; prov:wasDerivedFrom dgn-void:gad-20130706; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP96441.RAtMBDy-F_zpuiQrUNrwVfxb2b0DV0bStRYOl3T8oB6Ss130_publicationInfo { this: dcterms:created "2014-10-02T12:32:48+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" . }