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- NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_assertion type Assertion NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_head.
- NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_assertion wasGeneratedBy ECO_0000203 NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_provenance.
- NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_assertion wasDerivedFrom gad-20150221 NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_provenance.
- NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_assertion SIO_000772 20198651 NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_provenance.
- NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_assertion evidence source_evidence_literature NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_provenance.
- NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_assertion description "[Our data indicate that the FOXL2 codon 134 mutation occurs exclusively in GCT and thecoma, and suggest the possibility that the development of most GCTs and a fraction of thecomas may be dependent on this mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149891.RAqvnuP6m3MYbkf_TrPmawhIvOyedsq6UKm0JlUwtwLEE130_provenance.