Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_assertion type Assertion NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_head.
- NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_assertion description "[We conclude that ELAC2/HPC2 truncating mutations are rare in HPC, but that rare variants of the ELAC2/HPC2 require additional study as risk factors for PRCA in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_provenance.
- NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_assertion evidence source_evidence_literature NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_provenance.
- NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_assertion SIO_000772 11507049 NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_provenance.
- NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_assertion wasDerivedFrom befree-2016 NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_provenance.
- NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_assertion wasGeneratedBy ECO_0000203 NP327340.RAO1nSVODsx-j-1JqJZ_x7yuPGB9azs0GEHx9_TKDJPIc130_provenance.