@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:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_head { this: np:hasAssertion dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_assertion; np:hasProvenance dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_provenance; np:hasPublicationInfo dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_publicationInfo; a np:Nanopublication . dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_assertion a np:Assertion . dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_provenance a np:Provenance . dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_publicationInfo a np:PublicationInfo . } dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_assertion { miriam-gene:5521 a ncit:C16612 . lld:C0751781 a ncit:C7057 . dgn-gda:DGN4d45983f7add1e02cd6310ee20734986 sio:SIO_000628 miriam-gene:5521, lld:C0751781; a sio:SIO_001122 . } dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_provenance { dgn-np:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_assertion dcterms:description "[One hundred and forty-three families with dominantly inherited ataxia and 220 patients with apparently sporadic cerebellar ataxia were examined for the SCA1, SCA2, SCA3/Machado-Joseph disease (MJD), SCA6, SCA7, SCA8, SCA12 and dentatorubral-pallidoluysian atrophy (DRPLA) mutations.]. 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:12542511; 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:NP638846.RAggabfg1tGU_R-7X3DPjITMyUBFf6MbTtsMaxzrdriak130_publicationInfo { this: dcterms:created "2015-08-25T14:44:03+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" . }