Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_assertion wasGeneratedBy ECO_0000203 NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_assertion wasDerivedFrom befree-20140225 NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_assertion SIO_000772 19100507 NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_assertion evidence source_evidence_literature NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_assertion description "[When the overall frequencies of these chromosomal aberrations were distributed according to RAI stages, the majority of patients with 13q14.3 deletion (55%), trisomy 12 (70%), and ATM or TP53 deletions (66.7 %) were in advanced stages of disease (RAI II-IV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP393133.RA9nHetwJPRsDBHlf1XsFzl8w0O2CmJHw4hpmT2ziLFLY130_provenance.