Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_assertion type Assertion NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_head.
- NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_assertion description "[Deficiencies of coagulation factors other than factor VIII and factor IX (afibrinogenemia, FII, FV, FV+FVIII, FVII, FX, FXI, FXIII) that cause bleeding disorders (RBDs) are inherited as autosomal recessive traits and are rare, with prevalences in the general population varying between 1 in 500,000 and 1 in 2 million for the homozygous forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_provenance.
- NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_assertion evidence source_evidence_literature NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_provenance.
- NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_assertion SIO_000772 16684009 NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_provenance.
- NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_assertion wasDerivedFrom befree-2016 NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_provenance.
- NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_assertion wasGeneratedBy ECO_0000203 NP548803.RADYwNhNzRgGjdsXHZkFasKUGXTn8X96lDHDCqLyb6MgI130_provenance.