Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_assertion type Assertion NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_head.
- NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_assertion description "[Our data suggests that epilepsy may be a rare associated feature in children with muscular dystrophy secondary to dystrophin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_provenance.
- NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_assertion evidence source_evidence_literature NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_provenance.
- NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_assertion SIO_000772 10728205 NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_provenance.
- NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_assertion wasDerivedFrom befree-2016 NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_provenance.
- NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_assertion wasGeneratedBy ECO_0000203 NP278620.RACCO3mmNJgFdeT_i3IqxF6PheTX2tWYcwZ1j5RLdB9vA130_provenance.