Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_assertion> ?p ?o ?g. }
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- NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_assertion type Assertion NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_head.
- NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_assertion description "[Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_provenance.
- NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_assertion evidence source_evidence_literature NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_provenance.
- NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_assertion SIO_000772 25491320 NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_provenance.
- NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_assertion wasDerivedFrom befree-2016 NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_provenance.
- NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_assertion wasGeneratedBy ECO_0000203 NP1246522.RA4-SYB3k1VzTebbfzN99r5HhW2Gmut4QM6whfRQvaHFA130_provenance.