Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_assertion type Assertion NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_head.
- NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_assertion description "[Pompe disease is an autosomal recessive lysosomal glycogen storage disorder that has been reported in different ethnic populations which carry different common mutations of the acid alpha-glucosidase (GAA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_provenance.
- NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_assertion evidence source_evidence_literature NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_provenance.
- NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_assertion SIO_000772 25526786 NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_provenance.
- NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_assertion wasDerivedFrom befree-2016 NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_provenance.
- NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_assertion wasGeneratedBy ECO_0000203 NP1249812.RAIoyWdqTy9C4ZKQBqNepApFUCtNhVdILNsuxjYU7cg6s130_provenance.