Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP716435.RA1kwlhjq8UawFXKtk7-6-APtoaLpm-vmHSYXDq7jw6yU130_provenance.
- 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.