@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:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_head { this: np:hasAssertion dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_assertion; np:hasProvenance dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_provenance; np:hasPublicationInfo dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_publicationInfo; a np:Nanopublication . dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_assertion a np:Assertion . dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_provenance a np:Provenance . dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_assertion { miriam-gene:7273 a ncit:C16612 . lld:C0014072 a ncit:C7057 . dgn-gda:DGN89f7997118f52592d10d65f951abee9f sio:SIO_000628 miriam-gene:7273, lld:C0014072; a sio:SIO_001121 . } dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_provenance { dgn-np:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_assertion dcterms:description "[Here, we developed a novel therapeutic strategy to modulate the functions of RORγt using cell-transducible form of transcription modulation domain of RORγt (tRORγt-TMD), which can be delivered effectively into the nucleus of cells and into the central nerve system (CNS). tRORγt-TMD specifically inhibited TH17-related cytokines induced by RORγt, thereby suppressing the differentiation of naïve T cells into TH17, but not into TH1, TH2, or Treg cells. tRORγt-TMD injected into experimental autoimmune encephalomyelitis (EAE) animal model can be delivered effectively in the splenic CD4(+) T cells and spinal cord-infiltrating CD4(+) T cells, and suppress the functions of TH17 cells.]. 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:25527718; 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:NP1249957.RAdweIZO4sgR6nCYDJWB3aleSQgPR1GHjWW5wW08EwQnk130_publicationInfo { this: dcterms:created "2016-05-13T12:51:12+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" . }