Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_assertion description "[We propose that the combined beta-galactosidase/neuraminidase deficiency is caused by a defective 32,000-dalton glycoprotein which is normally required to protect beta-galactosidase and neuraminidase against excessive intralysosomal degradation and to give these enzymes their full hydrolytic activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_assertion evidence source_evidence_literature NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_assertion SIO_000772 6812049 NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_assertion wasDerivedFrom befree-20140225 NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_assertion wasGeneratedBy ECO_0000203 NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP308774.RA_ZWydoAORNo5hQ8jw7uJ_SzOWHj2TqOMixKy3DxsllE130_provenance.