@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:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_head { this: np:hasAssertion dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_assertion; np:hasProvenance dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_provenance; np:hasPublicationInfo dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_publicationInfo; a np:Nanopublication . dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_assertion a np:Assertion . dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_provenance a np:Provenance . dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_assertion { miriam-gene:348 a ncit:C16612 . lld:C0011265 a ncit:C7057 . dgn-gda:DGN581be033162bf5c360e1ee7bac681f83 sio:SIO_000628 miriam-gene:348, lld:C0011265; a sio:SIO_001121 . } dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_provenance { dgn-np:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_assertion dcterms:description "[The frequency of the APOE allele epsilon4 was similar in patients with Parkinson's disease and controls, but the APOE allele epsilon2, thought to be protective for dementia, was significantly more frequent in patients with sporadic Parkinson's disease than in 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:9328263; 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:NP1381843.RAq1R4ZXeYZHZI5Nr9inxKfIsPQbDGyjX1NfbbwS3hv8Y130_publicationInfo { this: dcterms:created "2016-05-13T12:52:12+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" . }