@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:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_head { this: np:hasAssertion dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_assertion; np:hasProvenance dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_provenance; np:hasPublicationInfo dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_publicationInfo; a np:Nanopublication . dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_assertion a np:Assertion . dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_provenance a np:Provenance . dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_assertion { miriam-gene:1038 a ncit:C16612 . lld:C0011265 a ncit:C7057 . dgn-gda:DGN7207890390bf14ad8061998e115ca402 sio:SIO_000628 miriam-gene:1038, lld:C0011265; a sio:SIO_001121 . } dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_provenance { dgn-np:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_assertion dcterms:description "[The baseline sample of 183 mutation carriers (MCs) and 117 noncarriers (NCs) was divided according to Clinical Dementia Rating (CDR) scale into preclinical (CDR 0; MCs: n = 107; NCs: n = 109), early symptomatic (CDR 0.5; MCs: n = 48; NCs: n = 8), and dementia stage (CDR ≥ 1; MCs: n = 28; NCs: n = 0).]. 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:25922840; 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:NP1281267.RAhHSMCRh-ouV1lA2UVV9zkQwq5_FrYGRjjLzYTv-AkWM130_publicationInfo { this: dcterms:created "2016-05-13T12:51:27+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" . }