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- NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_assertion type Assertion NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_head.
- NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_assertion wasGeneratedBy ECO_0000203 NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_provenance.
- NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_assertion wasDerivedFrom befree-20140225 NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_provenance.
- NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_assertion SIO_000772 20674321 NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_provenance.
- NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_assertion evidence source_evidence_literature NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_provenance.
- NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_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." NP770509.RA2q2pnjtP0dnuTow9-xtf6hj25M8thL2POWw68RZa2Dk130_provenance.