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Q31132884-6D61FCB1-E60A-495B-A7D7-AA06361BF793
Q31132884-6D61FCB1-E60A-495B-A7D7-AA06361BF793
BestRank
Statement
http://www.wikidata.org/entity/statement/Q31132884-6D61FCB1-E60A-495B-A7D7-AA06361BF793
Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.
P2860
Q31132884-6D61FCB1-E60A-495B-A7D7-AA06361BF793
BestRank
Statement
http://www.wikidata.org/entity/statement/Q31132884-6D61FCB1-E60A-495B-A7D7-AA06361BF793
rank
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type
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wasDerivedFrom
5c7d2662e1d6770a90466cbaeb7e17651def12fe
P2860
Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia.