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- source_evidence_literature type ECO_0000212 NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion wasGeneratedBy ECO_0000203 NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion wasDerivedFrom befree-20150227 NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion SIO_000772 20085575 NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion evidence source_evidence_literature NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion description "[The most frequent cytogenetic abnormalities were ETV6/RUNX1 fusion (16%) and trisomy 8 (14.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.