Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion> ?p ?o ?g. }
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- NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion type Assertion NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_head.
- NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion description "[Human erythrocyte R-type pyruvate kinase deficiency (PKD) is a disorder caused by mutations in the PKLR gene that produces chronic nonspherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_provenance.
- NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion evidence source_evidence_literature NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_provenance.
- NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion SIO_000772 19755962 NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_provenance.
- NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion wasDerivedFrom befree-20140225 NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_provenance.
- NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion wasGeneratedBy ECO_0000203 NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_provenance.