Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_assertion> ?p ?o ?g. }
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- NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_assertion type Assertion NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_head.
- NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_assertion wasGeneratedBy ECO_0000203 NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_provenance.
- NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_assertion wasDerivedFrom befree-2016 NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_provenance.
- NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_assertion SIO_000772 15358621 NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_provenance.
- NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_assertion evidence source_evidence_literature NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_provenance.
- NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_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." NP459278.RAPGfF0IQt1uM9_gVsXVut3jnJ_bGib-GdmXoTllxfVmA130_provenance.