@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:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_head { this: np:hasAssertion dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_assertion; np:hasProvenance dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_provenance; np:hasPublicationInfo dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_publicationInfo; a np:Nanopublication . dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_assertion a np:Assertion . dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_provenance a np:Provenance . dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_publicationInfo a np:PublicationInfo . } dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_assertion { miriam-gene:26278 a ncit:C16612 . lld:C0234132 a ncit:C7057 . dgn-gda:DGN980bca2dff99447899a35fd0882424d3 sio:SIO_000628 miriam-gene:26278, lld:C0234132; a sio:SIO_001121 . } dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_provenance { dgn-np:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_assertion dcterms:description "[With the collaboration of the clinical European and Mediterranean SPATAX network, we identified 15 families with 34 affected members presenting with ataxia and pyramidal signs or spasticity that were not linked to the ARSACS locus on chromosome 13.]. 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:17273843; 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:NP592047.RANjIKitdGazu0sNY4B28Q52gPvktsdhwWVrm7nEeeMtU130_publicationInfo { this: dcterms:created "2016-05-13T12:46:14+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }