Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_assertion description "[This specifically applies to children with severe congenital neutropenia who receive lifelong treatment with G-CSF and in which the high susceptibility to develop MDS and acute myeloid leukemia (AML) has now become a major clinical concern.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_assertion evidence source_evidence_literature NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_assertion SIO_000772 20237318 NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_assertion wasDerivedFrom befree-2016 NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_assertion wasGeneratedBy ECO_0000203 NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP800643.RA_mNRgWtiQ0AgF7R7tiISioYRsIMGICyr8A0vXW84HrQ130_provenance.