Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion> ?p ?o ?g. }
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- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion type Assertion NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_head.
- 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.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion evidence source_evidence_literature NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion SIO_000772 15892853 NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion wasDerivedFrom befree-20140225 NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.
- NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_assertion wasGeneratedBy ECO_0000203 NP299843.RAAevJmf8yVoxupcN846vstHHoH1QloK2GG8pHIWLN0eg130_provenance.