Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_assertion type Assertion NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_head.
- NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_assertion description "[Although a clinical overlap between patients with dominant and recessive RYR1 mutations exists, in most cases with recessive mutations the pattern of muscle weakness is remarkably different from that observed in dominant CCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_provenance.
- NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_assertion evidence source_evidence_literature NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_provenance.
- NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_assertion SIO_000772 17483490 NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_provenance.
- NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_assertion wasDerivedFrom befree-2016 NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_provenance.
- NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_assertion wasGeneratedBy ECO_0000203 NP608539.RATCoNukCpv1AzvBaIMYOBL7izMFrAmutw0_6VOOoSmYk130_provenance.