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- NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_assertion type Assertion NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_head.
- NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_assertion description "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_provenance.
- NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_assertion evidence source_evidence_literature NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_provenance.
- NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_assertion SIO_000772 17728323 NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_provenance.
- NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_assertion wasDerivedFrom befree-20140225 NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_provenance.
- NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_assertion wasGeneratedBy ECO_0000203 NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_provenance.