Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_assertion> ?p ?o ?g. }
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- NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_assertion type Assertion NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_head.
- NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_assertion description "[Two patients carried mutations in CEBPZ, suggesting that CEBPZ is a novel recurrently mutated gene in AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_provenance.
- NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_assertion evidence source_evidence_literature NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_provenance.
- NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_assertion SIO_000772 24923295 NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_provenance.
- NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_assertion wasDerivedFrom befree-2016 NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_provenance.
- NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_assertion wasGeneratedBy ECO_0000203 NP1191404.RAdyvXZWS7sDDOIJbK9Z-OuS8fRqZLDpPv5H4XPk16zWc130_provenance.