@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:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_head { this: np:hasAssertion dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_assertion; np:hasProvenance dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_provenance; np:hasPublicationInfo dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_publicationInfo; a np:Nanopublication . dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_assertion a np:Assertion . dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_provenance a np:Provenance . dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_publicationInfo a np:PublicationInfo . } dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_assertion { miriam-gene:4780 a ncit:C16612 . lld:C0002736 a ncit:C7057 . dgn-gda:DGN519b3762bd7f6d8c96d565568dfb6ab6 sio:SIO_000628 miriam-gene:4780, lld:C0002736; a sio:SIO_001121 . } dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_provenance { dgn-np:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_assertion dcterms:description "[Following this background, we expand our discussion to the role of Nrf2 in several major neurodegenerative disorders (NDDs) such as Alzheimer's disease, Parkinson's disease, Huntington's disease, multiple sclerosis and amyotrophic lateral sclerosis.]. 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:25280871; 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:NP1226137.RA6ZNhhufyLWwjrdWeTN02KR18YC1aUHYTQRzNlhphxWE130_publicationInfo { this: dcterms:created "2016-05-13T12:51:01+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" . }