Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_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." NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_assertion evidence source_evidence_literature NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_assertion SIO_000772 11230485 NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_assertion wasDerivedFrom befree-2016 NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_assertion wasGeneratedBy ECO_0000203 NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.
- befree-2016 importedOn "2016-02-19" NP309673.RA5QLPcO6sk4Tdu0M_MRof7Gs_088U9qkHGirp3dMrLtU130_provenance.