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- source_evidence_literature type ECO_0000212 NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_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." NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_assertion evidence source_evidence_literature NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_assertion SIO_000772 1991170 NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_assertion wasDerivedFrom befree-20150227 NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_assertion wasGeneratedBy ECO_0000203 NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP606039.RA31TUS7C5LWr_v1e4zm9xDXJ6qzP17Vp3xOf7Jwr4SyU130_provenance.