Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion type Assertion NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_head.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion wasGeneratedBy ECO_0000203 NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion wasDerivedFrom befree-20150227 NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion SIO_000772 22408652 NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion evidence source_evidence_literature NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion description "[Nearly all cases of FOP are caused by the identical mutation in the ACVR1 gene that causes a single amino acid substitution, R206H, in the bone morphogenetic protein (BMP) type I receptor ACVR1 (formerly known as ALK2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.