Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_assertion description "[Human beta-galactosidase and alpha-neuraminidase deficient mucolipidosis [ML(gal-neur-)] is an inherited lysosomal enzymopathy which recently was designated as a sialidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_assertion evidence source_evidence_literature NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_assertion SIO_000772 7076257 NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_assertion wasDerivedFrom befree-20140225 NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_assertion wasGeneratedBy ECO_0000203 NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP566484.RAUfzK3IZTYL5AmQNeHOHsilm0kEqwna1nUgRC9-ojzDE130_provenance.