@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:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_head { this: np:hasAssertion dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_assertion; np:hasProvenance dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_provenance; np:hasPublicationInfo dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_publicationInfo; a np:Nanopublication . dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_assertion a np:Assertion . dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_provenance a np:Provenance . dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_publicationInfo a np:PublicationInfo . } dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_assertion { miriam-gene:2876 a ncit:C16612 . lld:C1862939 a ncit:C7057 . dgn-gda:DGN4a56708b7f7c260c87277ffe28dad596 sio:SIO_000628 miriam-gene:2876, lld:C1862939; a sio:SIO_001122 . } dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_provenance { dgn-np:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_assertion dcterms:description "[To clarify the biological significance of the interaction of the redox system (Prx2/GPx1) with SOD1 in SOD1-mutated motor neurons in vivo, we produced an affinity-purified rabbit antibody against Prx2 and investigated the immunohistochemical localization of Prx2 and GPx1 in neuronal Lewy body-like hyaline inclusions (LBHIs) in the spinal cords of familial amyotrophic lateral sclerosis (FALS) patients with a two-base pair deletion at codon 126 and an Ala-->Val substitution at codon 4 in the SOD1 gene, as well as in transgenic rats expressing human SOD1 with H46R and G93A mutations.]. 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:14648077; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP433261.RAcsYBIlODHYGVZyOlU-ws9y2y0NM7Ix1po9mbSAIoLjc130_publicationInfo { this: dcterms:created "2015-08-25T14:41:52+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }