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- source_evidence_literature type ECO_0000212 NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_assertion description "[Absence of point mutations within the AML-1 gene in patients with MDS/AML and loss of chromosome 5q or 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_assertion evidence source_evidence_literature NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_assertion SIO_000772 11261327 NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_assertion wasDerivedFrom befree-2016 NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_assertion wasGeneratedBy ECO_0000203 NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.
- befree-2016 importedOn "2016-02-19" NP311725.RA1bBCFfxe0xnhOxEBMyjvsfPDBQ4xiy3zu17nEI42UuA130_provenance.