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- NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_assertion type Assertion NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_head.
- NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_assertion wasGeneratedBy ECO_0000203 NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_provenance.
- NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_assertion wasDerivedFrom befree-2016 NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_provenance.
- NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_assertion SIO_000772 11310626 NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_provenance.
- NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_assertion evidence source_evidence_literature NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_provenance.
- NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_assertion 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." NP315056.RA1_p9F-lupvYPjFQfH-UWha0vyN3xahWkdfhMT4zqnMA130_provenance.