Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_assertion> ?p ?o ?g. }
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- NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_assertion type Assertion NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_head.
- NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_assertion description "[Recent reports have suggested that Common Variable Immunodeficieny (CVID) can present as an autosomal dominant trait dependent on the inheritance of a set of uncommon mutations/alleles of TACI (transmembrane activator and calcium-modulator and cyclophilin ligand interactor) involving exons 3 or 4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_provenance.
- NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_assertion evidence source_evidence_literature NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_provenance.
- NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_assertion SIO_000772 19775471 NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_provenance.
- NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_assertion wasDerivedFrom befree-20140225 NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_provenance.
- NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_assertion wasGeneratedBy ECO_0000203 NP340800.RAEgP9ghTEeNOl5ZUByd4d-kOXnU9e2pzXcXA_jV04vbQ130_provenance.