@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:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_head { this: np:hasAssertion dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_assertion; np:hasProvenance dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_provenance; np:hasPublicationInfo dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_publicationInfo; a np:Nanopublication . dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_assertion a np:Assertion . dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_provenance a np:Provenance . dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_assertion { miriam-gene:1103 a ncit:C16612 . lld:C0002395 a ncit:C7057 . dgn-gda:DGN34f153ff7e7c4e08226d0877b0e54c9f sio:SIO_000628 miriam-gene:1103, lld:C0002395; a sio:SIO_001121 . } dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_provenance { dgn-np:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_assertion dcterms:description "[Although the magnitude of the cortical choline acetyltransferase deficit is comparable to that seen in the brains of patients with Alzheimer's disease, none of our OPCA patients appeared, on last examination, to have severe global dementia of the Alzheimer type.]. 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:3477997; 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:NP1302290.RAnbZa9eaU7M629_O22FjhQ3kni7Ydj2HhHz-ZR1qfKXM130_publicationInfo { this: dcterms:created "2016-05-13T12:51:36+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" . }