Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion type Assertion NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_head.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion description "[Mutations in myotilin gene (MYOT) have been associated with variable syndromes including limb girdle muscular dystrophy type 1A (LGMD1A) and a subgroup of myofibrillar myopathy (MFM/MYOT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion evidence source_evidence_literature NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion SIO_000772 15947064 NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion wasDerivedFrom befree-20140225 NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.
- NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_assertion wasGeneratedBy ECO_0000203 NP419560.RAUoXIXnel4NPdNYjui_cU095oImIq3gHrBXI-R2QCWdk130_provenance.