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- source_evidence_literature type ECO_0000212 NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_assertion description "[This includes cell lines derived from patients with relapsed disease featuring cytogenetic anomalies such as t(12;21), Philadelphia chromosome t(9;22), t(1;19) as well as a cell line carrying t(17;19) from a patient with de novo ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_assertion evidence source_evidence_literature NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_assertion SIO_000772 21960246 NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_assertion wasDerivedFrom befree-2016 NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_assertion wasGeneratedBy ECO_0000203 NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.
- befree-2016 importedOn "2016-02-19" NP927484.RAMj62Kkv3waUaL6Am1pqSWciVVGZsk1DW-YbZUiefqBo130_provenance.