Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_assertion> ?p ?o ?g. }
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- NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_assertion type Assertion NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_head.
- NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_assertion description "[1) Mutations in myotilin cause MFM; 2) exon 2 of MYOT is a hotspot for mutations; 3) peripheral neuropathy, cardiomyopathy, and distal weakness greater than proximal weakness are part of the spectrum of myotilinopathy; 4) not all cases of myotilinopathy have a limb-girdle phenotype; and 5) the molecular basis of the majority of MFM cases remains to be discovered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_provenance.
- NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_assertion evidence source_evidence_literature NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_provenance.
- NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_assertion SIO_000772 15111675 NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_provenance.
- NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_assertion wasDerivedFrom befree-2016 NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_provenance.
- NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_assertion wasGeneratedBy ECO_0000203 NP441637.RAdIwhndQA4uzKgk2Doxe94Mt3r6c6ZSnaFg20qNGOyhM130_provenance.