@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:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_head { this: np:hasAssertion dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_assertion; np:hasProvenance dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_provenance; np:hasPublicationInfo dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_publicationInfo; a np:Nanopublication . dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_assertion a np:Assertion . dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_provenance a np:Provenance . dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_publicationInfo a np:PublicationInfo . } dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_assertion { miriam-gene:773 a ncit:C16612 . lld:C0270749 a ncit:C7057 . dgn-gda:DGN5e59d95a4643c162cd08f6f8b3e6ac78 sio:SIO_000628 miriam-gene:773, lld:C0270749; a sio:SIO_001121 . } dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_provenance { dgn-np:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_assertion dcterms:description "[By means of transient linear acceleration of the whole body along the interaural axis, we examined the LVOR in six patients with hereditary cerebellar ataxia due to mutations of the calcium channel gene CACNA1A, five with spinocerebellar ataxia type 6 (SCA6) and one with episodic ataxia type 2 (EA-2).]. 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:11701595; 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:NP277078.RAweCv3z75rjRJ7gTDr_3zZKVXp5qbiGZwzEVplpvuBuY130_publicationInfo { this: dcterms:created "2015-08-25T14:40:18+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" . }