Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_assertion wasGeneratedBy ECO_0000203 NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_assertion wasDerivedFrom befree-20150227 NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_assertion SIO_000772 15358621 NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_assertion evidence source_evidence_literature NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.
- NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_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." NP294466.RAYUrOMM2pUVnK_bHYbYvqo18N11Dz44O7FS8uybaGUvo130_provenance.