Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_assertion> ?p ?o ?g. }
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- NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_assertion type Assertion NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_head.
- NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_assertion wasGeneratedBy ECO_0000218 NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_provenance.
- NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_assertion wasDerivedFrom uniprot-20130724 NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_provenance.
- NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_assertion SIO_000772 19344878 NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_provenance.
- NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_assertion evidence source_evidence_curated NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_provenance.
- NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_assertion description "[Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3943.RAcF7vL_cAG6NXdSgfG_jTcSCLFanUXIysas_U-2veWeo130_provenance.