Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_assertion> ?p ?o ?g. }
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- NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_assertion type Assertion NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_head.
- NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_assertion description "[Cori's disease is a glycogen storage disorder characterized by a deficiency in the glycogen debranching enzyme, amylo-1,6-glucosidase,4-alpha-glucanotransferase (AGL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_provenance.
- NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_assertion evidence source_evidence_literature NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_provenance.
- NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_assertion SIO_000772 17908927 NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_provenance.
- NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_assertion wasDerivedFrom befree-20140225 NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_provenance.
- NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_assertion wasGeneratedBy ECO_0000203 NP822648.RAaVspxxzlO2RdDFC34b2AE0EwKH7Scl--RXP1cw_xFpI130_provenance.