Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_assertion description "[We conclude that ras mutations are observed in childhood monosomy 7, though less frequently than in adult MDS, and may play a limited role in the progression of this disease to acute leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_assertion evidence source_evidence_literature NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_assertion SIO_000772 1991170 NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_assertion wasDerivedFrom befree-20150227 NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_assertion wasGeneratedBy ECO_0000203 NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781474.RA9pUHyGzoccI1HszcZQIxvtxj1YbMkfVN9j8M92mJN18130_provenance.