Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_assertion> ?p ?o ?g. }
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- NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_assertion type Assertion NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_head.
- NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_assertion description "[Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_provenance.
- NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_assertion evidence source_evidence_literature NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_provenance.
- NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_assertion SIO_000772 25524009 NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_provenance.
- NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_assertion wasDerivedFrom befree-2016 NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_provenance.
- NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_assertion wasGeneratedBy ECO_0000203 NP1249409.RAtP41gkIy8VuoTq5B4O2zMNi5bh4sKKPgXMo8rA89iS0130_provenance.