Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_assertion description "[Mutations with loss of heterozygosity of p53 are common in therapy-related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_assertion evidence source_evidence_literature NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_assertion SIO_000772 11230485 NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_assertion wasDerivedFrom befree-2016 NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_assertion wasGeneratedBy ECO_0000203 NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.
- befree-2016 importedOn "2016-02-19" NP309677.RAiHVTTHWHwBAvMgpO9_fhh4KqvJTAMPR00xs8s35MHdU130_provenance.