@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:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_head { this: np:hasAssertion dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_assertion; np:hasProvenance dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_provenance; np:hasPublicationInfo dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_publicationInfo; a np:Nanopublication . dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_assertion a np:Assertion . dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_provenance a np:Provenance . dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_assertion { miriam-gene:6310 a ncit:C16612 . lld:C0018790 a ncit:C7057 . dgn-gda:DGNad6281f5c5b18e3f4b783ebe7513c234 sio:SIO_000628 miriam-gene:6310, lld:C0018790; a sio:SIO_001122 . } dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_provenance { dgn-np:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_assertion dcterms:description "[We investigated the (CAG)n repeat length of the CACNL1A4 gene in 733 patients with sporadic ataxia and in 46 German families with dominantly inherited SCA which do not harbor the SCA1, SCA2, or MJD1/SCA3 mutation, respectively.]. 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:9259275; 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:NP1378666.RAtUXPSNaW6-BR3zFFNhpNuYLs8cDbK8K7zn0-b5mTvOY130_publicationInfo { this: dcterms:created "2016-05-13T12:52:10+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" . }