Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_assertion wasGeneratedBy ECO_0000203 NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_assertion wasDerivedFrom befree-20140225 NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_assertion SIO_000772 15358621 NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_assertion evidence source_evidence_literature NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_assertion description "[None of the remaining 33 patients (24 males/9 females) had mutations affecting CD40, ICOS, ICOSL, or SH2D1, and are best classified as common variable immune deficiency (CVID), although other genes, including some not yet identified, may be responsible.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP325798.RAsB2jGNPn-V9yRpMDcTNRj5B8dm6axzaS93uaGluMFE0130_provenance.