Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_assertion evidence source_evidence_literature NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_assertion SIO_000772 19917257 NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_assertion wasDerivedFrom befree-20140225 NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_assertion wasGeneratedBy ECO_0000203 NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.