Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_assertion description "[Recently, the authors discovered that the homozygous loss of the ICOS in humans presents as common variable immunodeficiency, the most prevalent treated primary immunodeficiency in man.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_assertion evidence source_evidence_literature NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_assertion SIO_000772 14612664 NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_assertion wasDerivedFrom befree-20150227 NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_assertion wasGeneratedBy ECO_0000203 NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP894572.RA0gJ_3Tex-XRLbNhL2NXWQg8QIK4CrSeQa5rh9zlhxbc130_provenance.