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- NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_assertion type Assertion NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_head.
- NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_assertion description "[Five missense mutations of the winged-helix FOXC1 transcription factor, found in patients with Axenfeld-Rieger (AR) malformations, were investigated for their effects on FOXC1 structure and function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_provenance.
- NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_assertion evidence source_evidence_literature NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_provenance.
- NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_assertion SIO_000772 11179011 NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_provenance.
- NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_assertion wasDerivedFrom befree-20140225 NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_provenance.
- NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_assertion wasGeneratedBy ECO_0000203 NP399703.RA5Q10fL24AgTJyoyoiduu1aTguxAuSyAZmSbaEbwf_Ro130_provenance.