Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_assertion> ?p ?o ?g. }
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- NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_assertion type Assertion NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_head.
- NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_assertion description "[Fabry's disease is an X linked inborn error of metabolism due to deficient activity of the lysosomal enzyme alpha galactosidase A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_provenance.
- NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_assertion evidence source_evidence_literature NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_provenance.
- NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_assertion SIO_000772 12185177 NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_provenance.
- NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_assertion wasDerivedFrom befree-20140225 NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_provenance.
- NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_assertion wasGeneratedBy ECO_0000203 NP474337.RADvoyt2cm1EPe11e0-E-bhxfl1ZW4W0iAIvwjutrlkWg130_provenance.