Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_assertion type Assertion NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_head.
- NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_assertion description "[We have identified mutations in an X chromosome-linked, Aristaless-related, homeobox gene (ARX), in nine families with mental retardation (syndromic and nonspecific), various forms of epilepsy, including infantile spasms and myoclonic seizures, and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_provenance.
- NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_assertion evidence source_evidence_literature NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_provenance.
- NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_assertion SIO_000772 11889467 NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_provenance.
- NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_assertion wasDerivedFrom befree-20140225 NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_provenance.
- NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_assertion wasGeneratedBy ECO_0000203 NP729924.RAB3W6Ac8puxDDMV1v2QPf9Ch94kpUAFHdiSvqd98saLk130_provenance.