Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion type Assertion NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_head.
- NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_provenance.
- NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion evidence source_evidence_literature NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_provenance.
- NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion SIO_000772 17635637 NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_provenance.
- NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion wasDerivedFrom befree-20140225 NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_provenance.
- NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_assertion wasGeneratedBy ECO_0000203 NP868144.RA0G5nHXWxpI29AUKVJZxRc14sNbydhTrEyYalWgYQd_0130_provenance.