@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:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_head { this: np:hasAssertion dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_assertion; np:hasProvenance dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_provenance; np:hasPublicationInfo dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_publicationInfo; a np:Nanopublication . dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_assertion a np:Assertion . dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_provenance a np:Provenance . dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_assertion { miriam-gene:348 a ncit:C16612 . lld:C0333641 a ncit:C7057 . dgn-gda:DGNb4b03644136a51a17d0366e05abfb01c sio:SIO_000628 miriam-gene:348, lld:C0333641; a sio:SIO_001122 . } dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_provenance { dgn-np:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_assertion dcterms:description "[Logopenic progressive aphasia and posterior cortical atrophy showed largely overlapping anatomic and biologic features with early age at onset of Alzheimer disease, suggesting that these clinical syndromes represent the spectrum of clinical manifestation]. 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:19901249; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP159921.RAQEqHRBFEQFDXYC01gU3Y2c10I9Qbi1g0x-fbTz6ko3Y130_publicationInfo { this: dcterms:created "2016-05-13T12:43:00+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" . }