Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_assertion> ?p ?o ?g. }
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- NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_assertion type Assertion NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_head.
- NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_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." NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_provenance.
- NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_assertion evidence source_evidence_literature NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_provenance.
- NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_assertion SIO_000772 9432020 NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_provenance.
- NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_assertion wasDerivedFrom befree-2016 NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_provenance.
- NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_assertion wasGeneratedBy ECO_0000203 NP1387019.RAcc6YCbkrM16pG0Lc2gmtqrt4zqeEUB21UbP4wZs4AHY130_provenance.