Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_assertion description "[Mutations with loss of function of p53 are significantly associated with deletion or loss of 5q in t-MDS and t-AML after previous treatment with alkylating agents and are associated with genetic instability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_assertion evidence source_evidence_literature NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_assertion SIO_000772 11230485 NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_assertion wasDerivedFrom befree-2016 NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_assertion wasGeneratedBy ECO_0000203 NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.
- befree-2016 importedOn "2016-02-19" NP309681.RARaLeIn1Hp15_dUxANA9xR-OoF7YpvXQ_qi2hiHuMnmc130_provenance.