Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion type Assertion NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_head.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion wasGeneratedBy ECO_0000203 NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion wasDerivedFrom befree-20140225 NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion SIO_000772 15776429 NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion evidence source_evidence_literature NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.
- NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_assertion description "[We screened the SIMPLE gene for mutations in a cohort of 192 patients with CMT or related neuropathies, each of whom tested negative for other known genetic causes of CMT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749721.RAK6n_hBpb6xG8Z0WAb0yu1bxCbFZcYp1Ux-j1mYa84RI130_provenance.