@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:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_head { this: np:hasAssertion dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_assertion; np:hasProvenance dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_provenance; np:hasPublicationInfo dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_publicationInfo; a np:Nanopublication . dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_assertion a np:Assertion . dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_provenance a np:Provenance . dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_publicationInfo a np:PublicationInfo . } dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_assertion { miriam-gene:5621 a ncit:C16612 . lld:C2936349 a ncit:C7057 . dgn-gda:DGNfb892abc5c5dcc87dbaa8192b0803c14 sio:SIO_000628 miriam-gene:5621, lld:C2936349; a sio:SIO_001121 . } dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_provenance { dgn-np:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_assertion dcterms:description "[Gerstmann-Sträussler-Scheinker syndrome (GSS) is a genetic prion disease typified clinically by the development of progressive ataxia and dementia, and histopathologically by the presence of prion protein (PrP) amyloid plaques in the CNS, especially within the cerebellum.]. 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:19675240; 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:NP757258.RAoD7vjQfnlpcqnLZxcaTbAqIvFfWD-SxyT9NppWvjW14130_publicationInfo { this: dcterms:created "2016-05-13T12:47:28+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" . }