Matches in Nanopublications for { ?s ?p "[Prothrombin deficiency is a rare (1:200 000) autosomal recessive disorder caused by diverse mutations in prothrombin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP265194.RAUcz9Pj5IrS3knbqSMqTL8NGGcTQIdCINFhTHddTJDHc130_assertion description "[Prothrombin deficiency is a rare (1:200 000) autosomal recessive disorder caused by diverse mutations in prothrombin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265194.RAUcz9Pj5IrS3knbqSMqTL8NGGcTQIdCINFhTHddTJDHc130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion description "[Prothrombin deficiency is a rare (1:200 000) autosomal recessive disorder caused by diverse mutations in prothrombin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.