Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_assertion> ?p ?o ?g. }
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- NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_assertion type Assertion NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_head.
- NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_assertion description "[Mutations in the genes of hematopoietic growth factor receptors as a cause of congenital cytopenia, such as congenital amegakaryocytic thrombocytopenia (CAMT) or severe congenital neutropenia (CN), are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_provenance.
- NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_assertion evidence source_evidence_literature NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_provenance.
- NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_assertion SIO_000772 11458519 NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_provenance.
- NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_assertion wasDerivedFrom befree-2016 NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_provenance.
- NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_assertion wasGeneratedBy ECO_0000203 NP324244.RACx3m3gEhBtiBDebStIglF1EMIHJHpdEo1X2iwHcTsJU130_provenance.