Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_assertion evidence source_evidence_literature NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_assertion SIO_000772 8985184 NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_assertion wasDerivedFrom befree-2016 NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_assertion wasGeneratedBy ECO_0000203 NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.