@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:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_head { this: np:hasAssertion dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_assertion; np:hasProvenance dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_provenance; np:hasPublicationInfo dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_publicationInfo; a np:Nanopublication . dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_assertion a np:Assertion . dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_provenance a np:Provenance . dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_publicationInfo a np:PublicationInfo . } dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_assertion { miriam-gene:1437 a ncit:C16612 . lld:C0030567 a ncit:C7057 . dgn-gda:DGNb61ad5b947839954136305cd7474e236 sio:SIO_000628 miriam-gene:1437, lld:C0030567; a sio:SIO_001121 . } dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_provenance { dgn-np:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_assertion dcterms:description "[The goal of the current investigation was to examine a cohort of symptomatic and asymptomatic LRRK2 mutation carriers, in order to address whether the reported alterations in amyloid β (Aβ) and tau species in the CSF of patients with sporadic Parkinson disease (PD) are a part of PD pathogenesis, the aging process, or a comorbid disease in patients with PD, and to explore the possibility of Aβ and tau as markers of early or presymptomatic PD.]. 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:22170881; 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:NP946812.RAe6neASyQ5wCxVHCc85EwGRCDfvwxdbMCIMUyZLeJqfE130_publicationInfo { this: dcterms:created "2016-05-13T12:48:54+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" . }