Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_assertion type Assertion NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_head.
- NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_assertion description "[Escobar syndrome has been recently described as a prenatal form of myasthenia associated with recessive mutations in genes of the neuromuscular junction (CHRNG, CHRNA1, CHRND, RAPSN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_provenance.
- NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_assertion evidence source_evidence_literature NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_provenance.
- NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_assertion SIO_000772 19155175 NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_provenance.
- NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_assertion wasDerivedFrom befree-20140225 NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_provenance.
- NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_assertion wasGeneratedBy ECO_0000203 NP679107.RAKQCaqU92twH0yThPRUvB0iQBtOEHuKzWAc7G3nhq1Z0130_provenance.