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- NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_assertion type Assertion NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_head.
- NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_assertion description "[A novel type 2A (Group II) von Willebrand disease mutation (L1503Q) associated with loss of the highest molecular weight von Willebrand factor multimers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_provenance.
- NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_assertion evidence source_evidence_literature NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_provenance.
- NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_assertion SIO_000772 15219197 NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_provenance.
- NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_assertion wasDerivedFrom befree-2016 NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_provenance.
- NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_assertion wasGeneratedBy ECO_0000203 NP449822.RAKyBBLrKC9swSLLaEjD-c4HIfgRj0Y3qmJbwfFiP8XFk130_provenance.