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- NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_assertion type Assertion NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_head.
- NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_assertion description "[Congenital central hypoventilation syndrome (CCHS), a rare disorder typically presenting in the newborn period, results in over 90% of cases from PHOX2B polyalanine repeat mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_provenance.
- NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_assertion evidence source_evidence_literature NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_provenance.
- NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_assertion SIO_000772 18340402 NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_provenance.
- NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_assertion wasDerivedFrom befree-2016 NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_provenance.
- NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_assertion wasGeneratedBy ECO_0000203 NP660678.RAc393090SJ0RvN6qA4DsKxLMLHKQ6q-M49gpQZCvtCRo130_provenance.