Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_assertion type Assertion NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_head.
- NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_assertion description "[These include lamin A/C in autosomal dominant Emery-Dreifuss muscular dystrophy, SMN in spinal muscular atrophy, SIX5 in myotonic dystrophy, calpain3 in type 2A limb-girdle muscular dystrophy, PABP2 in oculopharyngeal dystrophy, androgen receptor in spinal and bulbar muscular atrophy and the ataxins in hereditary ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_provenance.
- NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_assertion evidence source_evidence_literature NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_provenance.
- NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_assertion SIO_000772 10838245 NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_provenance.
- NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_assertion wasDerivedFrom befree-20140225 NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_provenance.
- NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_assertion wasGeneratedBy ECO_0000203 NP503302.RAhst7vkFq92z-4ItqQiucvX2vBG83IeF_qiLvG2p_9MU130_provenance.