Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion type Assertion NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_head.
- NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion description "[More recently, de novo missense mutations in the alpha-tubulin 1a gene (TUBA1A) located on chromosome 12q13.12, have also been associated with more or less severe defects of cortical development, resulting in complete agyria in the most severe cases of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_provenance.
- NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion evidence source_evidence_literature NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_provenance.
- NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion SIO_000772 20376468 NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_provenance.
- NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion wasDerivedFrom befree-20150227 NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_provenance.
- NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_assertion wasGeneratedBy ECO_0000203 NP841454.RAFYLtf18a-F-vhimXPJg6ifIdxe-beZ7RzM-Zby0yMCk130_provenance.