Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_assertion> ?p ?o ?g. }
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- NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_assertion type Assertion NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_head.
- NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_assertion wasGeneratedBy ECO_0000203 NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_provenance.
- NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_assertion wasDerivedFrom befree-20140225 NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_provenance.
- NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_assertion SIO_000772 15786463 NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_provenance.
- NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_assertion evidence source_evidence_literature NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_provenance.
- NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_assertion description "[The TRIM32 mutation found in the STM patients is identical to the causative mutation for LGMD2H (D487N), Haplotype analysis shows that the disease chromosomes share common ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516926.RA2wCmAzDluCKP9SNrhkMp5mkXQATfyEevWboaqMliW4Y130_provenance.