@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:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_head { this: np:hasAssertion dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_assertion; np:hasProvenance dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_provenance; np:hasPublicationInfo dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_publicationInfo; a np:Nanopublication . dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_assertion a np:Assertion . dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_provenance a np:Provenance . dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_publicationInfo a np:PublicationInfo . } dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_assertion { miriam-gene:2896 a ncit:C16612 . lld:C0524851 a ncit:C7057 . dgn-gda:DGNd4b076921aaf665b85c5be42fc8a4cb7 sio:SIO_000628 miriam-gene:2896, lld:C0524851; a sio:SIO_001122 . } dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_provenance { dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_assertion dcterms:description "[To assess the influence of rs5848 and rs646776 polymorphisms in both serum GRN level and risk for common neurodegenerative diseases, we studied 304 patients with Parkinson's disease (PD), 217 individuals with Alzheimer's disease, 131 subjects with mild cognitive impairment, and 126 controls.]. 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:23398167; 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:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_publicationInfo { this: dcterms:created "2016-05-13T12:49:43+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" . }