@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:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_head { this: np:hasAssertion dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_assertion; np:hasProvenance dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_provenance; np:hasPublicationInfo dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_publicationInfo; a np:Nanopublication . dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_assertion a np:Assertion . dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_provenance a np:Provenance . dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_publicationInfo a np:PublicationInfo . } dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_assertion { miriam-gene:4548 a ncit:C16612 . lld:C3711850 a ncit:C7057 . dgn-gda:DGNd2e187b41e56b8e535a335050276b985 sio:SIO_000628 miriam-gene:4548, lld:C3711850; a sio:SIO_001121 . } dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_provenance { dgn-np:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_assertion dcterms:description "[This form of MS generally has a higher age at onset and a higher female to male ratio than conventional MS. Opticospinal MS is also characterised by frequent relapses, severe disability, few brain lesions visible on MRI, long lesions extending over many vertebral segments visible on spinal-cord MRI, pleocytosis and an absence of oligoclonal bands in the CSF, and a pronounced shift in the responses of T-helper-1 and T-cytotoxic-1 cells throughout relapse and remission phases.]. 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:12849268; 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:NP577523.RAM_NRKz3IaUnOuVQKjNE3UR8CQHqc5ob2nN2tifldMks130_publicationInfo { this: dcterms:created "2015-08-25T14:43:24+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" . }