Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_assertion> ?p ?o ?g. }
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- NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_assertion type Assertion NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_head.
- NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_assertion description "[A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_provenance.
- NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_assertion evidence source_evidence_literature NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_provenance.
- NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_assertion SIO_000772 24793135 NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_provenance.
- NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_assertion wasDerivedFrom befree-2016 NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_provenance.
- NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_assertion wasGeneratedBy ECO_0000203 NP1179091.RASIkgsEu0t0E-Qg7WcERu1W_tIWgsB2C85ErylWdXKTk130_provenance.