Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_assertion description "[We describe the long-time course of 2 brothers with the familial chylomicronemia syndrome caused by identical compound heterozygous mutations in the lipoprotein lipase (LPL) gene with markedly reduced LPL activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_assertion evidence source_evidence_literature NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_assertion SIO_000772 16552344 NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_assertion wasDerivedFrom befree-2016 NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_assertion wasGeneratedBy ECO_0000203 NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.
- befree-2016 importedOn "2016-02-19" NP541453.RAfF1KKU8k_Dtmo8mI7cBxJI3h3v0s7brGPTKLaLxLn34130_provenance.