Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_assertion description "[A novel MLH1 mutation harbored as a germ line aberration by a young woman of an HNPCC-like family and exhibited by a CML patient when occurring prior to the initiation of the blast phase concomitant with a c-MYC amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_assertion evidence source_evidence_literature NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_assertion SIO_000772 16685411 NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_assertion wasDerivedFrom befree-2016 NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_assertion wasGeneratedBy ECO_0000203 NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.
- befree-2016 importedOn "2016-02-19" NP548959.RAgc3nP99oxKuX9SpTxtaqJ6Gp_G7XpvUR-FA0gOSLDtg130_provenance.