Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_assertion> ?p ?o ?g. }
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- NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_assertion type Assertion NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_head.
- NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_assertion wasGeneratedBy ECO_0000203 NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_provenance.
- NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_assertion wasDerivedFrom befree-20140225 NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_provenance.
- NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_assertion SIO_000772 14967765 NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_provenance.
- NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_assertion evidence source_evidence_literature NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_provenance.
- NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_assertion description "[At the same time, this progress blurs the traditional boundaries between the categories of congenital and limb-girdle muscular dystrophies, as well as between limb-girdle muscular dystrophies and other clinical entities, as mutations in genes such as fukutin-related protein, dysferlin, caveolin-3 and lamin A/C can cause a striking variety of phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621477.RA_2X-FeRwk-pl-ZtKHVOxCVcIaLy26OaPWbPs0idR9X8130_provenance.