Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_assertion> ?p ?o ?g. }
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- NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_assertion type Assertion NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_head.
- NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_assertion description "[Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-? deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_provenance.
- NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_assertion evidence source_evidence_literature NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_provenance.
- NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_assertion SIO_000772 25492228 NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_provenance.
- NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_assertion wasDerivedFrom befree-2016 NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_provenance.
- NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_assertion wasGeneratedBy ECO_0000203 NP1246637.RAfC2Gq0eydYJa_WUankDn9I-QHI75PnAOxnucBlYi2xE130_provenance.