Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_assertion description "[Using a heterologous expression system, we show that GPD1L associated with SCN5A and that the BrS- and SIDS-related mutations in GPD1L caused a loss of enzymatic function resulting in glycerol-3-phosphate PKC-dependent phosphorylation of SCN5A at serine 1503 (S1503) through a GPD1L-dependent pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_assertion evidence source_evidence_literature NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_assertion SIO_000772 19666841 NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_assertion wasDerivedFrom befree-20150227 NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_assertion wasGeneratedBy ECO_0000203 NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP869618.RAjE1jA1WrobpndW5gWxoFeq5rrwX-vzMeECC8U15aREc130_provenance.