Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_assertion type Assertion NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_head.
- NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_assertion wasGeneratedBy ECO_0000203 NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_provenance.
- NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_assertion wasDerivedFrom befree-20140225 NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_provenance.
- NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_assertion SIO_000772 20674321 NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_provenance.
- NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_assertion evidence source_evidence_literature NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_provenance.
- NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_assertion description "[By contrast, CMC is one of the few key infections in patients with autosomal dominant hyper IgE syndrome (mutations in STAT3), and in rare patients with autosomal recessive predisposition to mucocutaneous and invasive fungal infections (mutation in CARD9).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913354.RAQ_LD7w06oHc4Kg5x1PTIo9KRJ4zQfPVcrQtsPB5Ji_U130_provenance.