Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_assertion type Assertion NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_head.
- NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_assertion description "[HIES are a group of primary immunodeficiencies with overlapping and distinct features, most frequently caused by deficiency in signal transducer and activator of transcription 3 (STAT3) or dedicator of cytokinesis 8 (DOCK8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_provenance.
- NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_assertion evidence source_evidence_literature NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_provenance.
- NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_assertion SIO_000772 25469836 NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_provenance.
- NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_assertion wasDerivedFrom befree-2016 NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_provenance.
- NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_assertion wasGeneratedBy ECO_0000203 NP1244387.RACgEQMQ_pfMd3ixlMurogopLpXsXYEqA1aUJeY1t56I4130_provenance.