@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:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_head { this: np:hasAssertion dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_assertion; np:hasProvenance dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_provenance; np:hasPublicationInfo dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_publicationInfo; a np:Nanopublication . dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_assertion a np:Assertion . dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_provenance a np:Provenance . dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_publicationInfo a np:PublicationInfo . } dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_assertion { miriam-gene:1471 a ncit:C16612 . lld:C2931784 a ncit:C7057 . dgn-gda:DGN2fdcf466e9a9b704ef31f59fa5e2e846 sio:SIO_000628 miriam-gene:1471, lld:C2931784; a sio:SIO_001121 . } dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_provenance { dgn-np:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_assertion dcterms:description "[Two forms of inherited intracerebral hemorrhage (ICH) are associated with an amyloid angiopathy caused by mutations in the genes for the amyloid precursor protein or cystatin C. The purpose of this study was to determine whether patients with sporadic ICH have mutations in the amyloid precursor protein or cystatin C genes.]. 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:7945009; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP333613.RAkCCaqxNyX45dOo2mD0XGLhODYxpxkq0E7juk3gcZqrs130_publicationInfo { this: dcterms:created "2015-08-25T14:40:52+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }