@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:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_head { this: np:hasAssertion dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_assertion; np:hasProvenance dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_provenance; np:hasPublicationInfo dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_publicationInfo; a np:Nanopublication . dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_assertion a np:Assertion . dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_provenance a np:Provenance . dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_publicationInfo a np:PublicationInfo . } dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_assertion { miriam-gene:1270 a ncit:C16612 . lld:C0026769 a ncit:C7057 . dgn-gda:DGN427005a17720c824b449ca7ef2466a26 sio:SIO_000628 miriam-gene:1270, lld:C0026769; a sio:SIO_001121 . } dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_provenance { dgn-np:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_assertion dcterms:description "[Recent studies in new EAE models, especially in transgenic ones, have in connection with new analytical techniques such as microarray assays provided a deeper insight into the pathogenic cellular and molecular mechanisms of EAE and potentially of MS. For example, it was possible to better delineate the role of soluble pro-inflammatory (tumor necrosis factor-α, interferon-γ and interleukins 1, 12 and 23), anti-inflammatory (transforming growth factor-β and interleukins 4, 10, 27 and 35) and neurotrophic factors (ciliary neurotrophic factor and brain-derived neurotrophic factor).]. 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:20558237; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP720290.RAtP4_kJhYCELGplbOa9c8i1bPc_-AHP6vWfK_RoULkgM130_publicationInfo { this: dcterms:created "2014-10-02T12:39:17+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" . }