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- NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_assertion type Assertion NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_head.
- NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_assertion wasGeneratedBy ECO_0000203 NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_provenance.
- NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_assertion wasDerivedFrom befree-2016 NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_provenance.
- NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_assertion SIO_000772 15492925 NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_provenance.
- NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_assertion evidence source_evidence_literature NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_provenance.
- NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_assertion description "[Rett syndrome (RTT) is a severe neurodevelopmental disorder caused, in most classic cases, by mutations in the X-linked methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465322.RARlEmk1oTPlQymU6_i-bMsNJJeGEWE2HkEb7jLvpNav8130_provenance.