Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_assertion type Assertion NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_head.
- NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_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." NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_provenance.
- NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_assertion evidence source_evidence_literature NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_provenance.
- NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_assertion SIO_000772 15219197 NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_provenance.
- NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_assertion wasDerivedFrom gad-20150221 NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_provenance.
- NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_assertion wasGeneratedBy ECO_0000203 NP86346.RARI0gfKDUVECzHSeBhDnXcaegChvdMxedJyeW0f5Q-OI130_provenance.