@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:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_head { this: np:hasAssertion dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_assertion; np:hasProvenance dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_provenance; np:hasPublicationInfo dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_publicationInfo; a np:Nanopublication . dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_assertion a np:Assertion . dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_provenance a np:Provenance . dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_publicationInfo a np:PublicationInfo . } dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_assertion { miriam-gene:3736 a ncit:C16612 . lld:C1719788 a ncit:C7057 . dgn-gda:DGN00f4733b7365e00d9f0c93eb1dd6144a sio:SIO_000628 miriam-gene:3736, lld:C1719788; a sio:SIO_001121 . } dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_provenance { dgn-np:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_assertion dcterms:description "[We excluded linkage to 11 regions containing genes associated with chorea and myokymia: 1) the Huntington disease gene on chromosome 4p; 2) the paroxysmal dystonic choreoathetosis gene at 2q34; 3) the dentatorubral-pallidoluysian atrophy gene at 12p13; 4) the choreoathetosis/spasticity disease locus on 1p that lies in a region containing a cluster of potassium (K+) channel genes; 5) the episodic ataxia type 1 (EA1) locus on 12p that contains the KCNA1 gene and two other voltage-gated K+ channel genes, KCNA5 and KCNA6; 6) the chorea-acanthocytosis locus on 9q21; 7) the Huntington-like syndrome on 20p; 8) the paroxysmal kinesigenic dyskinesia locus on 16p11.2-q11.2; 9) the benign hereditary chorea locus on 14q; 10) the SCA type 5 locus on chromosome 11; and 11) the chromosome 19 region that contains several ion channels and the CACNA1A gene, a brain-specific P/Q-type calcium channel gene associated with ataxia and hemiplegic migraine.]. 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:11310626; 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:NP315058.RAY6cWx-YypwVpU3AoMwomImnTgiwf8ttOp05jTxgi5LI130_publicationInfo { this: dcterms:created "2016-05-13T12:44:08+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" . }