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- NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_assertion type Assertion NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_head.
- NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_provenance.
- NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_assertion evidence source_evidence_curated NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_provenance.
- NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_assertion SIO_000772 22158539 NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_provenance.
- NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_assertion wasDerivedFrom ctd_human-2016 NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_provenance.
- NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_assertion wasGeneratedBy ECO_0000218 NP30503.RA5_RYO_cPIjODVfARRnJNwVNUdVCklbuNiWaxFR-S2QQ130_provenance.