Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- befree-2016 importedOn "2016-02-19" NP829733.RAQOSSxA_qm9LR2A_s5GoYwmnvYcI7Dg1hsnE1yahwdTs130_provenance.
- 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.