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- source_evidence_literature type ECO_0000212 NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_assertion description "[Although signalling deregulation is involved in CMML, transcriptional deregulation seems to play a pivotal role, with mutation of RUNX1, ASXL1 or TET2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_assertion evidence source_evidence_literature NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_assertion SIO_000772 20955399 NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_assertion wasDerivedFrom befree-2016 NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_assertion wasGeneratedBy ECO_0000203 NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.
- befree-2016 importedOn "2016-02-19" NP846460.RAbkqHt8KwA4UoR3fW1E2FNGZ_XVUP9tMJ4ODGulDnQZA130_provenance.