Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion type Assertion NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_head.
- NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion description "[the mutation in prothrombin that may have a role in hereditary prothrombin deficiency in Indian patients is named'Prothrombin Vellore 1'and is an Ala362Thr mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.
- NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion evidence source_evidence_literature NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.
- NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion SIO_000772 15892853 NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.
- NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion wasDerivedFrom lhgdn-20090331 NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.
- NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_assertion wasGeneratedBy ECO_0000203 NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.