@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:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_head { this: np:hasAssertion dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_assertion; np:hasProvenance dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_provenance; np:hasPublicationInfo dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_publicationInfo; a np:Nanopublication . dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_assertion a np:Assertion . dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_provenance a np:Provenance . dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_publicationInfo a np:PublicationInfo . } dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_assertion { miriam-gene:6712 a ncit:C16612 . lld:C0018790 a ncit:C7057 . dgn-gda:DGNfbcfcd8c638ea488e896fb23f0909949 sio:SIO_000628 miriam-gene:6712, lld:C0018790; a sio:SIO_001121 . } dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_provenance { dgn-np:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_assertion dcterms:description "[While locus homogeneity with SCA5 is not formally excluded, we consider it rather unlikely on phenotypic grounds, and propose that this condition may represent an addition to the group of neurogenetic disorders subsumed under the rubric SCA.]. 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:14998916; 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:NP434023.RAK-jM4AFQdEiPJSmAhL7PqctfRRG6iPLauhvWygpOlvI130_publicationInfo { this: dcterms:created "2016-05-13T12:45:02+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" . }