Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_assertion type Assertion NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_head.
- NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_assertion description "[Recent studies have demonstrated that hypomorphic mutations in signal transducer and activator of transcription 3 result in the classical multisystem form of HIES, whereas a null mutation in tyrosine kinase 2 causes the autosomal recessive form of HIES that is associated with viral and mycobacterial infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_provenance.
- NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_assertion evidence source_evidence_literature NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_provenance.
- NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_assertion SIO_000772 19088064 NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_provenance.
- NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_assertion wasDerivedFrom befree-20150227 NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_provenance.
- NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_assertion wasGeneratedBy ECO_0000203 NP716431.RAGr8N5381mlyGvLpHBdo0ICsMYjqZKWfxjHCOG_bJvUc130_provenance.