Matches in Nanopublications for { ?s ?p "[A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP383.RAPzxr8kfjJS0IvJaeUkxjQ3s1cz29UmCePllPZS2YSvE130_assertion description "[A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383.RAPzxr8kfjJS0IvJaeUkxjQ3s1cz29UmCePllPZS2YSvE130_provenance.
- NP3194.RAZrf3T5Jk6P6qJNQLS5K2fiIns-b81bhzTs9y7G2SJro130_assertion description "[A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3194.RAZrf3T5Jk6P6qJNQLS5K2fiIns-b81bhzTs9y7G2SJro130_provenance.
- NP1204.RAR53ObUYtJQfZ9U_pnumgATZQuLDDYJZ0Q_BWaNOjcgU130_assertion description "[A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1204.RAR53ObUYtJQfZ9U_pnumgATZQuLDDYJZ0Q_BWaNOjcgU130_provenance.