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- source_evidence_literature type ECO_0000212 NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP210843.RARejzVXZskgs_0G_vl4t5bu3y5W_gT9AjF3Cc7c82v_k130_provenance.