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- source_evidence_literature type ECO_0000212 NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_assertion description "[Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_assertion evidence source_evidence_literature NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_assertion SIO_000772 1829836 NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_assertion wasDerivedFrom befree-2016 NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_assertion wasGeneratedBy ECO_0000203 NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.
- befree-2016 importedOn "2016-02-19" NP657249.RAdzLulLnYikrVRW_lRg3BiJjgZhtPaBtn18QXIZYPonM130_provenance.