Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_assertion type Assertion NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_head.
- NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_assertion wasGeneratedBy ECO_0000203 NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_assertion wasDerivedFrom befree-2016 NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_assertion SIO_000772 20674321 NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_assertion evidence source_evidence_literature NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_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." NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.