Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_assertion> ?p ?o ?g. }
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- NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_assertion type Assertion NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_head.
- NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_assertion description "[The authors assessed ARX as a candidate gene for XLAG in a genetic analysis of neuronal migration disorders and found two different point mutations in two XLAG pedigrees affecting the homeodomain of the protein, confirming that ARX is a causative gene for XLAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_provenance.
- NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_assertion evidence source_evidence_literature NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_provenance.
- NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_assertion SIO_000772 12874405 NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_provenance.
- NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_assertion wasDerivedFrom befree-20140225 NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_provenance.
- NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_assertion wasGeneratedBy ECO_0000203 NP473957.RAvRnD9rIa1bxmqC3npmFeo1QcNGKR6h4WFBEWB3FRyvY130_provenance.