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- source_evidence_literature type ECO_0000212 NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_assertion description "[Inactivating or dominant-negative mutations in the RUNX1 gene have been also identified in pedigrees of familial platelet disorders with a variable propensity to develop acute myeloid leukemia (FPD/AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_assertion evidence source_evidence_literature NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_assertion SIO_000772 21725049 NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_assertion wasDerivedFrom befree-2016 NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_assertion wasGeneratedBy ECO_0000203 NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP906724.RAmK5NjJR5t1zfcUpFKZ9vuacBvbxouE7MjMmupo-9TWU130_provenance.