@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:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_head { this: np:hasAssertion dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_assertion; np:hasProvenance dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_provenance; np:hasPublicationInfo dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_publicationInfo; a np:Nanopublication . dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_assertion a np:Assertion . dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_provenance a np:Provenance . dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_publicationInfo a np:PublicationInfo . } dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_assertion { miriam-gene:4854 a ncit:C16612 . lld:C0011265 a ncit:C7057 . dgn-gda:DGN51bc23ce9daa4a0a31595405529ef9a5 sio:SIO_000628 miriam-gene:4854, lld:C0011265; a sio:SIO_001121 . } dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_provenance { dgn-np:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_assertion dcterms:description "[We here report the case of a 69-year-old woman with recurrent transient ischemic attacks (TIAs) and strokes, seizures, and dementia without any mutations in exons 3 and 4 of the Notch3 gene and with a normal skin biopsy, but who showed characteristic CADASIL abnormalities on brain pathological examination.]. 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:11718749; 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:NP337105.RA4oatfHl8bcqUrOwU0J6zQul9lFNWRUnSY5hQsoE3de0130_publicationInfo { this: dcterms:created "2016-05-13T12:44:18+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" . }