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- NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_assertion type Assertion NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_head.
- NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_assertion description "[The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_provenance.
- NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_assertion evidence source_evidence_literature NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_provenance.
- NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_assertion SIO_000772 25720245 NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_provenance.
- NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_assertion wasDerivedFrom befree-2016 NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_provenance.
- NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_assertion wasGeneratedBy ECO_0000203 NP1266486.RAeCyzq8Nu_dLFrC-7NM0gIEXrxR8M3ZRH_YwmJ9z_5qw130_provenance.