Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_assertion> ?p ?o ?g. }
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- NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_assertion type Assertion NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_head.
- NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_assertion description "[We looked at 4 patients with severe and unusual infections in whom MBP gene mutations were the only identified cause of immunodeficiency and one patient with combined MBP and IgA deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_provenance.
- NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_assertion evidence source_evidence_literature NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_provenance.
- NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_assertion SIO_000772 7707811 NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_provenance.
- NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_assertion wasDerivedFrom befree-20140225 NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_provenance.
- NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_assertion wasGeneratedBy ECO_0000203 NP473239.RA5W89b7w9-eCcv-WltHnsQV52Lx-3wUlpbglEoOwK4Ac130_provenance.