Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion> ?p ?o ?g. }
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- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion type Assertion NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_head.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion evidence source_evidence_literature NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion SIO_000772 10496225 NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion wasDerivedFrom befree-2016 NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.
- NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_assertion wasGeneratedBy ECO_0000203 NP263791.RAym4YlYb7W7pPX4fho-0jI0HWz20ZplQWQtM4dVZcW7A130_provenance.