Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_assertion description "[The disease relapsed shortly after the treatment, and the karyotype analysis revealed a complex abnormality accompanied with t(9;11)(p22;q23), however, monosomy 7 was absent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_assertion evidence source_evidence_literature NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_assertion SIO_000772 12537982 NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_assertion wasDerivedFrom befree-20140225 NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_assertion wasGeneratedBy ECO_0000203 NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900497.RAeyGFHF4M-peoXtmD02yThf_fbrLScQokMyXDmtfcbaM130_provenance.