Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_assertion> ?p ?o ?g. }
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- NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_assertion type Assertion NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_head.
- NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_assertion description "[Curiously, although the index patient inherited both Bernard Soulier syndrome and factor XI deficiency (FXI: C = 1.3%), he had mild bleeding symptoms restricted only to ecchymoses and petechiae.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_provenance.
- NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_assertion evidence source_evidence_literature NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_provenance.
- NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_assertion SIO_000772 15823864 NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_provenance.
- NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_assertion wasDerivedFrom befree-2016 NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_provenance.
- NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_assertion wasGeneratedBy ECO_0000203 NP489421.RA_t6zG8QBcdYSkvS9gGNrFsiaCSUXRjvgNKy5rTC9AwM130_provenance.