Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_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." NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_assertion evidence source_evidence_literature NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_assertion SIO_000772 20237318 NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_assertion wasDerivedFrom befree-20150227 NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_assertion wasGeneratedBy ECO_0000203 NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP331935.RAduzzfMop_w0HoD0h9__8IbeOmjA-v7d737pC5WMyfvc130_provenance.