Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_assertion> ?p ?o ?g. }
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- NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_assertion type Assertion NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_head.
- NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_assertion wasGeneratedBy ECO_0000203 NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_provenance.
- NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_assertion wasDerivedFrom lhgdn-20090331 NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_provenance.
- NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_assertion SIO_000772 15786463 NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_provenance.
- NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_assertion evidence source_evidence_literature NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_provenance.
- NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_assertion description "[TRIM32 mutation found in the sarcotubular myopathy patients is identical to the causative mutation for LGMD2H (D487N) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209918.RA6CuMzUSiK7a-0E0LMGmSXSkQx51NcK_v592BDzWP7Zs130_provenance.