Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_assertion type Assertion NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_head.
- NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_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." NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_provenance.
- NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_assertion evidence source_evidence_literature NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_provenance.
- NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_assertion SIO_000772 15921228 NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_provenance.
- NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_assertion wasDerivedFrom befree-2016 NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_provenance.
- NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_assertion wasGeneratedBy ECO_0000203 NP496778.RA5g9GLCsQzmj7LGPwKktbNo2jWgV0jRfhotxgcpP3Mzc130_provenance.