Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_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." NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_assertion evidence source_evidence_literature NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_assertion SIO_000772 24793135 NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_assertion wasDerivedFrom befree-20150227 NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_assertion wasGeneratedBy ECO_0000203 NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP624066.RAtgmWkAe_1Yh62BcjZCqgw4lUIzoMHLOMjc1eoPOp-3k130_provenance.