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Q28198461-F22A9414-0A84-498C-99DC-B6BD304F8525
Q28198461-F22A9414-0A84-498C-99DC-B6BD304F8525
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28198461-F22A9414-0A84-498C-99DC-B6BD304F8525
A novel deafness/dystonia peptide gene mutation that causes dystonia in female carriers of Mohr-Tranebjaerg syndrome
P2860
Q28198461-F22A9414-0A84-498C-99DC-B6BD304F8525
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28198461-F22A9414-0A84-498C-99DC-B6BD304F8525
rank
NormalRank
type
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Statement
wasDerivedFrom
2974e7c3e43f334489cb9f16acb5012a0adfd624
P2860
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia