Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_assertion> ?p ?o ?g. }
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- NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_assertion type Assertion NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_head.
- NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_assertion wasGeneratedBy ECO_0000203 NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_provenance.
- NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_assertion wasDerivedFrom befree-20140225 NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_provenance.
- NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_assertion SIO_000772 7655856 NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_provenance.
- NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_assertion evidence source_evidence_literature NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_provenance.
- NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_assertion description "[Among glycolytic enzyme defects, hexokinase (ATP: D-hexose 6-phosphotransferase, EC 2.7.1.1; HK) deficiency is a very rare disease where the predominant clinical effect is nonspherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938578.RAcANgsWKxmnSexbcGVlIo3ge2VJ4umQD_2P0aAzW2LBA130_provenance.