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- NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_assertion type Assertion NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_head.
- NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_assertion wasGeneratedBy ECO_0000203 NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_provenance.
- NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_assertion wasDerivedFrom befree-20150227 NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_provenance.
- NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_assertion SIO_000772 23403440 NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_provenance.
- NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_assertion evidence source_evidence_literature NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_provenance.
- NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_assertion description "[LIPA gene mutations result in deficiency of lysosomal acid lipase and present phenotypically as Wolman disease or cholesteryl ester storage disease (CESD) depending on the level of deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849594.RACPjHFjyMoXlKJx-75pKL34aul3ISHlev_ttdrlz6iL0130_provenance.