Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion> ?p ?o ?g. }
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- NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion type Assertion NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_head.
- NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_provenance.
- NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion evidence source_evidence_literature NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_provenance.
- NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion SIO_000772 8755644 NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_provenance.
- NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion wasDerivedFrom gad-20150221 NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_provenance.
- NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_assertion wasGeneratedBy ECO_0000203 NP59937.RAouDm8raFz0vArHrGDDdjJJDjLl_pnzHfqlfyaqUuxKc130_provenance.