Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_assertion> ?p ?o ?g. }
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- NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_assertion type Assertion NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_head.
- NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_assertion wasGeneratedBy ECO_0000203 NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_assertion wasDerivedFrom befree-20150227 NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_assertion SIO_000772 20674321 NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_assertion evidence source_evidence_literature NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_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." NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.