Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_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." NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_assertion evidence source_evidence_literature NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_assertion SIO_000772 24793135 NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_assertion wasDerivedFrom befree-20150227 NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_assertion wasGeneratedBy ECO_0000203 NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP232365.RALgo4_UZ8YCsjXamt8OXMlkl8nVS9LHe8LNOAIWDc-A8130_provenance.