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Q33576895-16EC0F19-2BD3-4BE0-9E6E-605FB10F5A84
Q33576895-16EC0F19-2BD3-4BE0-9E6E-605FB10F5A84
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33576895-16EC0F19-2BD3-4BE0-9E6E-605FB10F5A84
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
P478
Q33576895-16EC0F19-2BD3-4BE0-9E6E-605FB10F5A84
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33576895-16EC0F19-2BD3-4BE0-9E6E-605FB10F5A84
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
333c2aa55fcabf48e87ec2c47e489481022b4ea5
P478
60
http://www.w3.org/2001/XMLSchema#string