Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_assertion type Assertion NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_head.
- NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior subcortical band heterotopia owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_provenance.
- NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_assertion evidence source_evidence_literature NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_provenance.
- NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_assertion SIO_000772 15921228 NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_provenance.
- NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_assertion wasDerivedFrom befree-2016 NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_provenance.
- NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_assertion wasGeneratedBy ECO_0000203 NP496787.RAMYYK19BdSkgsZ80B6Jkg2eRUxa5Y8C91Sr2euIPWcI8130_provenance.