Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_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." NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_assertion evidence source_evidence_literature NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_assertion SIO_000772 1991170 NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_assertion wasDerivedFrom befree-20140225 NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_assertion wasGeneratedBy ECO_0000203 NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP292192.RAN79wDSZgqpOL93akQ1L75vgW0xkClt3fYGoIEfP6HUQ130_provenance.