@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:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_head { this: np:hasAssertion dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_assertion; np:hasProvenance dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_provenance; np:hasPublicationInfo dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_publicationInfo; a np:Nanopublication . dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_assertion a np:Assertion . dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_provenance a np:Provenance . dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_publicationInfo a np:PublicationInfo . } dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_assertion { miriam-gene:65055 a ncit:C16612 . lld:C3711370 a ncit:C7057 . dgn-gda:DGN32942f8043e98c4662cbccceda2da405 sio:SIO_000628 miriam-gene:65055, lld:C3711370; a sio:SIO_001122 . } dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_provenance { dgn-np:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_assertion dcterms:description "[We screened 135 unrelated index cases, selected in five different settings: SPG7-positive patients detected during SPG31 analysis using SPG31/SPG7 multiplex ligation-dependent probe amplification (n = 7); previously reported ambiguous SPG7 cases (n = 5); patients carefully selected on the basis of their phenotype (spasticity of the lower limbs with cerebellar signs and/or cerebellar atrophy on magnetic resonance imaging/computer tomography scan and/or optic neuropathy and without other signs) (n = 24); patients with hereditary spastic paraparesis referred consecutively from attending neurologists and the national reference centre in a diagnostic setting (n = 98); and the index case of a four-generation family with autosomal dominant optic neuropathy but no spasticity linked to the SPG7 locus.]. 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:23065789; 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:NP940664.RAilTlV8mMpseaAPB44-aNMM--eTJ9pxDx19_uBwQxVQg130_publicationInfo { this: dcterms:created "2015-08-25T14:47:14+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" . }