Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion> ?p ?o ?g. }
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- NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion type Assertion NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_head.
- NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_provenance.
- NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion evidence source_evidence_literature NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_provenance.
- NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion SIO_000772 10938133 NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_provenance.
- NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion wasDerivedFrom befree-20140225 NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_provenance.
- NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion wasGeneratedBy ECO_0000203 NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_provenance.