Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_assertion> ?p ?o ?g. }
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- NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_assertion type Assertion NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_head.
- NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_assertion description "[A point mutation responsible for human erythrocyte AMP deaminase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_provenance.
- NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_assertion evidence source_evidence_curated NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_provenance.
- NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_assertion SIO_000772 8004104 NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_provenance.
- NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_assertion wasDerivedFrom uniprot-20130724 NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_provenance.
- NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_assertion wasGeneratedBy ECO_0000218 NP380.RAwc2xVPjD6Qnch9BsRWyKRJTG5WNVuWQfCXbHcNNbmiY130_provenance.