Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_assertion type Assertion NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_head.
- NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_assertion description "[Here, we describe activated PI3K-I' syndrome (APDS), a PID associated with a dominant gain-of-function mutation in which lysine replaced glutamic acid at residue 1021 (E1021K) in the p110I' protein, the catalytic subunit of phosphoinositide 3-kinase I' (PI3KI'), encoded by the PIK3CD gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_provenance.
- NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_assertion evidence source_evidence_curated NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_provenance.
- NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_assertion SIO_000772 24136356 NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_provenance.
- NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_assertion wasDerivedFrom uniprot-20150221 NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_provenance.
- NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_assertion wasGeneratedBy ECO_0000218 NP39.RAdyA7Ve805TE4WyAnO_fDllXvGIpid1yrADx9Cpt3W8U130_provenance.