Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion type Assertion NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_head.
- NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_provenance.
- NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion evidence source_evidence_literature NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_provenance.
- NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion SIO_000772 18925516 NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_provenance.
- NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion wasDerivedFrom befree-20140225 NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_provenance.
- NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_assertion wasGeneratedBy ECO_0000203 NP247178.RAKjCkQqwWimQJBr2F7zQGWM38KXPrjb2fEzP_mEM_zSo130_provenance.