Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion type Assertion NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_head.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion description "[Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion evidence source_evidence_literature NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion SIO_000772 9432020 NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion wasDerivedFrom befree-20150227 NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.
- NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_assertion wasGeneratedBy ECO_0000203 NP231769.RAj2z7TneRkuQhiEVpXJSTZenCwvfMK0m44Eho-WEX4lY130_provenance.